Proposed Information Collection Activity; Comment Request, 18908-18909 [2017-08167]
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18908
Federal Register / Vol. 82, No. 77 / Monday, April 24, 2017 / Notices
jstallworth on DSK7TPTVN1PROD with NOTICES
Control Act (12 U.S.C. 1817(j)) and
§ 225.41 of the Board’s Regulation Y (12
CFR 225.41) to acquire shares of a bank
or bank holding company. The factors
that are considered in acting on the
notices are set forth in paragraph 7 of
the Act (12 U.S.C. 1817(j)(7)).
The notices are available for
immediate inspection at the Federal
Reserve Bank indicated. The notices
also will be available for inspection at
the offices of the Board of Governors.
Interested persons may express their
views in writing to the Reserve Bank
indicated for that notice or to the offices
of the Board of Governors. Comments
must be received not later than May 9,
2017.
A. Federal Reserve Bank of Dallas
(Robert L. Triplett III, Senior Vice
President) 2200 North Pearl Street,
Dallas, Texas 75201–2272:
1. Asif M. Dakri and Faizel M. Dakri,
Houston, Texas; to acquire voting shares
of Wallis Bancshares, Inc. (‘‘Wallis
Bancshares’’), Houston, Texas, and
thereby indirectly acquire voting shares
of Wallis State Bank, Wallis, Texas; and
Musa A. Dakri, Asif M. Dakri, Faizel M.
Dakri, the Dakri Family 2012 GST Trust
for Asif M. Dakri, and the Dakri Family
2012 GST Trust for Faizel M. Dakri, all
of Houston Texas, as a group acting in
concert, to acquire voting shares of
Wallis Bancshares.
B. Federal Reserve Bank of
Minneapolis (Jacquelyn K. Brunmeier,
Assistant Vice President) 90 Hennepin
Avenue, Minneapolis, Minnesota
55480–0291:
1. James Richard Sankovitz, Chaska,
Minnesota; individually and as trustee
of the Irrevocable Trust Agreement for
the benefit of Katherine M. Buland
(‘‘Buland Trust’’), to acquire voting
shares of Frankson Investment
Corporation (‘‘Frankson’’), and thereby
indirectly acquire shares of The First
National Bank of Waseca, all of Waseca,
Minnesota; and the Buland Trust (James
Sankovitz, Thomas Sankovitz, and Ann
Gaytko, as trustees) and Bernard Gaytko,
Waseca, Minnesota, to retain voting
shares of Frankson and join the
Sankovitz family shareholder group
which was previously approved to
control Frankson, as a group acting in
concert.
Board of Governors of the Federal Reserve
System, April 18, 2017.
Ann E. Misback,
Secretary of the Board.
FEDERAL RESERVE SYSTEM
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The applications listed below, as well
as other related filings required by the
Board, are available for immediate
inspection at the Federal Reserve Bank
indicated. The applications will also be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
(12 U.S.C. 1843). Unless otherwise
noted, nonbanking activities will be
conducted throughout the United States.
Unless otherwise noted, comments
regarding each of these applications
must be received at the Reserve Bank
indicated or the offices of the Board of
Governors not later than May 18, 2017.
A. Federal Reserve Bank of St. Louis
(David L. Hubbard, Senior Manager)
P.O. Box 442, St. Louis, Missouri
63166–2034. Comments can also be sent
electronically to
Comments.applications@stls.frb.org:
1. M1 Bancshares, Inc., Macks Creek,
Missouri; to become a bank holding
company by acquiring 100 percent of
the voting shares of The Bank of Macks
Creek, Macks Creek, Missouri.
Board of Governors of the Federal Reserve
System, April 18, 2017.
Ann E. Misback,
Secretary of the Board.
[FR Doc. 2017–08149 Filed 4–21–17; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Title: Implementation Grants to
Develop a Model Intervention for
Youth/Young Adults with Child Welfare
Involvement at Risk of Homelessness:
Phase II.
OMB No.: 0970–0445.
Description: The Administration for
Children and Familes (ACF) at the U.S.
Department of Health and Human
Services (HHS) intends to collect data
for an evaluation of the initiative,
Implementation Grants to Develop a
Model Intervention for Youth/Young
Adults with Child Welfare Involvement
at Risk of Homelessness: Phase II. This
builds on the previously approved
‘‘Planning Grants to Develop a Model
Intervention for Youth/Young Adults
with Child Welfare Involvement at Risk
of Homelessness’’ (Phase I). Phase II is
an initiative, funded by the Children’s
Bureau (CB) within ACF, that will
support implementation grants for
interventions designed to intervene with
youth who have experienced time in
foster care and are most likely to have
a challenging transition into adulthood,
including homelessness and unstable
housing experiences. CB awarded six
implementation grants (Phase II) in
September 2015. During the
implementation phase, organizations
will conduct a range of activities to finetune their comprehensive service
model, determine whether their model
is being implemented as intended, and
develop plans to evaluate the model
under a potential future funding
opportunity (Phase III).
During Phase II, ACF will engage a
contractor to conduct a cross-site
process evaluation. Data collected for
the process evaluation will be used to
assess grantees’ organizational capacity
to implement and evaluate the model
interventions and to monitor each
grantee’s progress toward achieving the
goals of the implementation period.
Data for the process evaluation will be
collected through interviews during site
visits.
Respondents: Grantee agency
directors and staff; partner agency
directors and staff. Partner agencies may
vary by site, but are expected to include
child welfare, mental health, and youth
housing/homelessness agencies.
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18909
Federal Register / Vol. 82, No. 77 / Monday, April 24, 2017 / Notices
ANNUAL BURDEN ESTIMATES
Total/annual
number of
respondents
Instrument
Communications for site visit planning ............................................................
Discussion guide: Individual and small-group interviews ................................
Estimated Total Annual Burden
Hours: 96.
Additional Information: Copies of the
proposed collection may be obtained by
writing to the Administration for
Children and Families, Office of
Planning, Research and Evaluation, 330
C Street SW., Washington, DC 20201,
Attn: OPRE Reports Clearance Officer.
All requests should be identified by the
title of the information collection. Email
address: OPREinfocollection@
acf.hhs.gov.
OMB Comment: OMB is required to
make a decision concerning the
collection of information between 30
and 60 days after 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 collection should
be sent directly to the following: Office
of Management and Budget, Paperwork
Reduction Project, Email: OIRA_
SUBMISSION@OMB.EOP.GOV, Attn:
Desk Officer for the Administration for
Children and Families.
Mary Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2017–08167 Filed 4–21–17; 8:45 am]
BILLING CODE 4184–29–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2017–N–0001]
Gastroenterology and Urology Devices
Panel of the Medical Devices Advisory
Committee; Notice of Meeting
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) announces a
forthcoming public advisory committee
meeting of the Gastroenterology and
Urology Devices Panel of the Medical
Devices Advisory Committee. The
general function of the committee is to
provide advice and recommendations to
the Agency on FDA’s regulatory issues.
The meeting will be open to the public.
jstallworth on DSK7TPTVN1PROD with NOTICES
SUMMARY:
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60
The meeting will be held on May
17, 2017, from 8 a.m. to 6 p.m.
ADDRESSES: Hilton Washington, DC/
North, Salons A, B, C, and D, 620 Perry
Pkwy., Gaithersburg, MD 20877. The
hotel’s telephone number is 301–977–
8900. Answers to commonly asked
questions including information
regarding special accommodations due
to a disability, visitor parking, and
transportation may be accessed at:
https://www.fda.gov/Advisory
Committees/AboutAdvisoryCommittees/
ucm408555.htm.
DATES:
FOR FURTHER INFORMATION CONTACT:
Patricio G. Garcia, Center for Devices
and Radiological Health, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 66, Rm. G610, Silver Spring,
MD 20993–0002, Patricio.Garcia@
fda.hhs.gov, 301–796–6875, or FDA
Advisory Committee Information Line,
1–800–741–8138 (301–443–0572 in the
Washington, DC area). A notice in the
Federal Register about last minute
modifications that impact a previously
announced advisory committee meeting
cannot always be published quickly
enough to provide timely notice.
Therefore, you should always check the
Agency’s Web site at https://www.fda.
gov/AdvisoryCommittees/default.htm
and scroll down to the appropriate
advisory committee meeting link, or call
the advisory committee information line
to learn about possible modifications
before coming to the meeting.
SUPPLEMENTARY INFORMATION:
Agenda: On May 17, 2017, the
committee will discuss, make
recommendations, and vote on
information regarding the premarket
approval application (PMA) for the
TRANSMEDICS ORGAN CARE
SYSTEM (OCS)—Lung System, by
TransMedics, Inc. The proposed
Indication for Use, as stated in the PMA,
is as follows: The TRANSMEDICS
ORGAN CARE SYSTEM (OCS) Lung
System is a portable organ perfusion,
ventilation, and monitoring medical
device intended to preserve donor lungs
in a near physiologic, ventilated, and
perfused state for transplantation.
FDA intends to make background
material available to the public no later
than 2 business days before the meeting.
If FDA is unable to post the background
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Number of
responses per
respondent
1
1
Average
burden hours
per response
1
1.5
Total/annual
burden hours
6
90
material on its Web site prior to the
meeting, the background material will
be made publicly available at the
location of the advisory committee
meeting, and the background material
will be posted on FDA’s Web site after
the meeting. Background material is
available at https://www.fda.gov/
AdvisoryCommittees/Calendar/
default.htm. Scroll down to the
appropriate advisory committee meeting
link.
Procedure: Interested persons may
present data, information, or views,
orally or in writing, on issues pending
before the committee. Written
submissions may be made to the contact
person on or before May 8, 2017. Oral
presentations from the public will be
scheduled between approximately 1
p.m. and 2 p.m. Those individuals
interested in making formal oral
presentations should notify the contact
person and submit a brief statement of
the general nature of the evidence or
arguments they wish to present, the
names and addresses of proposed
participants, and an indication of the
approximate time requested to make
their presentation on or before April 28,
2017. Time allotted for each
presentation may be limited. If the
number of registrants requesting to
speak is greater than can be reasonably
accommodated during the scheduled
open public hearing session, FDA may
conduct a lottery to determine the
speakers for the scheduled open public
hearing session. The contact person will
notify interested persons regarding their
request to speak by May 1, 2017.
Persons attending FDA’s advisory
committee meetings are advised that the
Agency is not responsible for providing
access to electrical outlets.
FDA welcomes the attendance of the
public at its advisory committee
meetings and will make every effort to
accommodate persons with disabilities.
If you require accommodations due to a
disability, please contact Artair Mallett
at artair.mallett@fda.hhs.gov or 301–
796–9638 at least 7 days in advance of
the meeting.
FDA is committed to the orderly
conduct of its advisory committee
meetings. Please visit our Web site at
https://www.fda.gov/Advisory
Committees/AboutAdvisoryCommittees/
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Agencies
[Federal Register Volume 82, Number 77 (Monday, April 24, 2017)]
[Notices]
[Pages 18908-18909]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-08167]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Title: Implementation Grants to Develop a Model Intervention for
Youth/Young Adults with Child Welfare Involvement at Risk of
Homelessness: Phase II.
OMB No.: 0970-0445.
Description: The Administration for Children and Familes (ACF) at
the U.S. Department of Health and Human Services (HHS) intends to
collect data for an evaluation of the initiative, Implementation Grants
to Develop a Model Intervention for Youth/Young Adults with Child
Welfare Involvement at Risk of Homelessness: Phase II. This builds on
the previously approved ``Planning Grants to Develop a Model
Intervention for Youth/Young Adults with Child Welfare Involvement at
Risk of Homelessness'' (Phase I). Phase II is an initiative, funded by
the Children's Bureau (CB) within ACF, that will support implementation
grants for interventions designed to intervene with youth who have
experienced time in foster care and are most likely to have a
challenging transition into adulthood, including homelessness and
unstable housing experiences. CB awarded six implementation grants
(Phase II) in September 2015. During the implementation phase,
organizations will conduct a range of activities to fine-tune their
comprehensive service model, determine whether their model is being
implemented as intended, and develop plans to evaluate the model under
a potential future funding opportunity (Phase III).
During Phase II, ACF will engage a contractor to conduct a cross-
site process evaluation. Data collected for the process evaluation will
be used to assess grantees' organizational capacity to implement and
evaluate the model interventions and to monitor each grantee's progress
toward achieving the goals of the implementation period. Data for the
process evaluation will be collected through interviews during site
visits.
Respondents: Grantee agency directors and staff; partner agency
directors and staff. Partner agencies may vary by site, but are
expected to include child welfare, mental health, and youth housing/
homelessness agencies.
[[Page 18909]]
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Total/annual Number of Average burden
Instrument number of responses per hours per Total/annual
respondents respondent response burden hours
----------------------------------------------------------------------------------------------------------------
Communications for site visit planning.......... 6 1 1 6
Discussion guide: Individual and small-group 60 1 1.5 90
interviews.....................................
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 96.
Additional Information: Copies of the proposed collection may be
obtained by writing to the Administration for Children and Families,
Office of Planning, Research and Evaluation, 330 C Street SW.,
Washington, DC 20201, Attn: OPRE Reports Clearance Officer. All
requests should be identified by the title of the information
collection. Email address: OPREinfocollection@acf.hhs.gov.
OMB Comment: OMB is required to make a decision concerning the
collection of information between 30 and 60 days after 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 collection should be sent directly to the following: Office
of Management and Budget, Paperwork Reduction Project, Email:
OIRA_SUBMISSION@OMB.EOP.GOV, Attn: Desk Officer for the Administration
for Children and Families.
Mary Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2017-08167 Filed 4-21-17; 8:45 am]
BILLING CODE 4184-29-P