Federal Register / Vol. 70, No.

46 / Thursday, March 10, 2005 / Notices 11985

Annualized Table:

Average bur-
Number of re-
Number of re- den per re-
Respondents sponses per
spondents sponse
respondent (in hours)

3rd Year Medical Students .......................................................................................................... 850 1 25/60

Dated: March 3, 2005. Comments are invited on: (a) Whether the nation’s use of inpatient medical
Betsey Dunaway, the proposed collection of information and surgical care provided in short-stay,
Acting Reports Clearance Officer, Office of is necessary for the proper performance non-Federal hospitals. The NSAS is a
the Chief Science Officer, Centers for Disease of the functions of the agency, including national probability sample survey of
Control and Prevention. whether the information shall have ambulatory surgery visits in hospitals
[FR Doc. 05–4684 Filed 3–9–05; 8:45 am] practical utility; (b) the accuracy of the and freestanding ambulatory surgery
BILLING CODE 4163–18–P agency’s estimate of the burden of the centers. It has been the benchmark
proposed collection of information; (c) against which special programmatic
ways to enhance the quality, utility, and data sources are compared.
DEPARTMENT OF HEALTH AND clarity of the information to be Data for the NSAS will be collected
HUMAN SERVICES collected; and (d) ways to minimize the annually beginning in 2006 from a
burden of the collection of information nationally representative sample of
Centers for Disease Control and on respondents, including through the hospitals and freestanding ambulatory
Prevention use of automated collection techniques surgery centers. The hospital universe
[60Day–05BK] or other forms of information includes noninstitutional hospitals
technology. Written comments should exclusive of Federal, military, and
Proposed Data Collections Submitted be received within 60 days of this Department of Veterans Affairs hospitals
for Public Comment and notice. located in the 50 States and the District
Recommendations of Columbia. The universe of
Proposed Project
In compliance with the requirement freestanding facilities includes the
of section 3506(c)(2)(A) of the National Survey of Ambulatory freestanding ambulatory surgery centers
Paperwork Reduction Act of 1995 for Surgery (OMB No. 0920–0334)— licensed by states and/or certified as
opportunity for public comment on Reinstatement—National Center for ambulatory surgery centers for Medicare
proposed data collection projects, the Health Statistics (NCHS), Centers for reimbursement. As in the earlier survey,
Centers for Disease Control and Disease Control and Prevention (CDC). facilities specializing in dentistry,
Prevention (CDC) will publish periodic The National Survey of Ambulatory podiatry, abortion, family planning or
summaries of proposed projects. To Surgery (NSAS) was previously birthing will be excluded. As with
request more information on the conducted by the CDC National Center previous years, the data items which are
proposed projects or to obtain a copy of for Health Statistics from 1994 through abstracted from medical records are the
the data collection plans and 1996. It is the principal source of data basic core variables from the Uniform
instruments, call (404) 371–5976 or on ambulatory surgery center (ASC) Hospital Discharge Data Set (UHDDS) as
send comments to Sandi Gambescia, services in the United States. It well as surgery times, total charges and
CDC Assistant Reports Clearance complements surgery data obtained in information on anesthesia. There are no
Officer, 1600 Clifton Road, MS–D74, the NCHS National Hospital Discharge costs to respondents except for their
Atlanta, GA 30333 or send an e-mail to Survey (NHDS) OMB No. 0920–0212, time to participate in the survey.
omb@cdc.gov. which provides annual data concerning Annualized Burden Table:

Number of re- Avg. burden/

Number of re- Total burden
Respondents sponses/re- response (in
spondents hours
spondent hrs.)

Induction1 ......................................................................................................... 227 1 90/60 340.5

Out-of-scope verification .................................................................................. 150 1 4/60 10
Sample Listing Sheet:
ASC Personnel ......................................................................................... 224 12 30/60 1,344
Census Personnel .................................................................................... 264 12 0 0
Medical Abstract:
ASC Personnel ......................................................................................... 324 250 12/60 16,200
Census Personnel .................................................................................... 164 250 2/60 1,367
Annual Update ................................................................................................. 488 1 5/60 41
Quality Control ................................................................................................. 245 20 2/60 163

Total .......................................................................................................... ........................ ........................ ........................ 19,465.5

1 The induction of 600 facilities takes place in the first year and 40 each in subsequent years but is averaged over 3 years.

VerDate jul<14>2003 18:28 Mar 09, 2005 Jkt 205001 PO 00000 Frm 00058 Fmt 4703 Sfmt 4703 E:\FR\FM\10MRN1.SGM 10MRN1
 11986 Federal Register / Vol. 70, No. 46 / Thursday, March 10, 2005 / Notices
Dated: March 1, 2005.
Betsey Dunaway,
Acting Reports Clearance Officer, Office of
the Chief Science Officer, Centers for Disease
Control and Prevention.
[FR Doc. 05–4687 Filed 3–9–05; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Information Collections Related
to Reunification Procedures for
Unaccompanied Alien Children.
OMB No.: New collection.
Description: Following the passage of
the 2002 Homeland Security Act (Pub.
L. 107–296), the Administration for
Instrument
Sponsor’s Agreement ....................................................................................
Verification of Release ...................................................................................
Family Reunification Packet ..........................................................................
Authorization for Release of Information .......................................................
Estimated Total Annual Burden
Hours: 5,800.
Additional Information: Copies of the
proposed collections may be obtained
by writing to the Administration for
Children and Families, Office of
Administration, Office of Information
Services, 370 L’Enfant Promenade, SW.,
Washington, DC 20447, Attn: ACF
Reports Clearance Officer. All requests
should be identified by the title of the
information collection. E-mail address:
grjohnsno@acf.hhs.gov.
OMB Comment: OMB is required to
make a decision concerning the
collection of information between 30
and 60 days after the publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect if OMB receives it
within 30 days of publication. Written
comments and recommendations for the
proposed information collections
should be sent directly to the following:
Office of Management and Budget,
Paperwork Reduction Project, Attn:
Desk Officer for ACF. E-mail address:
Katherine T. Astrich@omb.eop.gov.
VerDate jul<14>2003 18:28 Mar 09, 2005 Jkt 205001
Children and Families (ACF), Office of
Refugee Resettlement (ORR), is charged
with the care and placement of
unaccompanied alien children in
Federal custody, and implementing a
policy for the release of these children,
when appropriate, upon the request of
suitable sponsors while awaiting
immigration proceedings. In order for
ORR to make determinations regarding
the release of these children, the
potential sponsors must meet certain
conditions pursuant to section 462 of
the Homeland Security Act and the
Flores v. Reno Settlement Agreement
No. CV85–4544–RJK (C.D. Cal. 1997).
ORR considers the suitability of a
sponsor based on the sponsor’s ability
and agreement to provide for the
physical, mental and financial well-
being of an unaccompanied minor and
assurance to appear before immigration
courts. To ensure the safety of the
children, sponsors must undergo a
ANNUAL BURDEN ESTIMATES
Number of
respondents
Dated: March 4, 2005.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 05–4692 Filed 3–9–05; 8:45 am]
BILLING CODE 4184–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket Nos. 2004M–0538, 2004M–0495,
2004M–0450, 2004M–0467, 2004M–0471,
2004M–0533, 2004M–0496, 2004M–0497]
Medical Devices; Availability of Safety
and Effectiveness Summaries for
Premarket Approval Applications
AGENCY: Food and Drug Administration,
HHS.
ACTION: Notice.
SUMMARY: The Food and Drug
Administration (FDA) is publishing a
list of premarket approval applications
(PMAs) that have been approved. This
list is intended to inform the public of
the availability of safety and
effectiveness summaries of approved
PMAs through the Internet and the
agency’s Division of Dockets
Management.
PO 00000 Frm 00059 Fmt 4703 Sfmt 4703
background check. Suitable sponsors
may be parents, close relatives, friends
or entities concerned with the child’s
welfare. In this Notice, ACF announces
that it proposes to employ the use of
several information collections for
recording: (1) The Sponsor’s Agreement
to Conditions of Release, which collects
the sponsor’s affirmation to the terms of
the release; (2) the Verification of
Release, which collects the children’s
affirmation to the terms of their release;
(3) the Family Reunification Packet,
which collects information related to
the sponsor’s ability to provide for the
physical, mental and financial well-
being of the child(ren) and (4) the
Authorization for Release of
Information, which collects information
to be utilized for a background check.
Respondents: Potential sponsors of
unaccompanied alien children and
unaccompanied alien children in
Federal custody.
Number of Average Total
responses per burden hours burden
respondent per response hours
3,000 1 .166666 500
3,000 1 .166666 500
3,000 20 .05 3,000
3,000 12 .05 1,800
ADDRESSES: Submit written requests for
copies of summaries of safety and
effectiveness to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. Please cite
the appropriate docket number as listed
in table 1 of this document when
submitting a written request. See the
SUPPLEMENTARY INFORMATION section for
electronic access to the summaries of
safety and effectiveness.
FOR FURTHER INFORMATION CONTACT:
Thinh Nguyen, Center for Devices and
Radiological Health (HFZ–402), Food
and Drug Administration, 9200
Corporate Blvd., Rockville, MD 20850,
301–594–2186.
SUPPLEMENTARY INFORMATION:
I. Background
In the Federal Register of January 30,
1998 (63 FR 4571), FDA published a
final rule that revised 21 CFR 814.44(d)
and 814.45(d) to discontinue individual
publication of PMA approvals and
denials in the Federal Register. Instead,
the agency now posts this information
on the Internet on FDA’s home page at
http://www.fda.gov. FDA believes that
this procedure expedites public
notification of these actions because
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