Information Collection Being Submitted for Review and Approval to the Office of Management and Budget, 55199 [2016-19741]
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Federal Register / Vol. 81, No. 160 / Thursday, August 18, 2016 / Notices
Dated: July 27, 2016.
James D. Giattina,
Director, Water Protection Division.
fcc.gov and to Cathy.Williams@fcc.gov.
Include in the comments the OMB
control number as shown in the
SUPPLEMENTARY INFORMATION section
below.
[FR Doc. 2016–19099 Filed 8–17–16; 8:45 am]
BILLING CODE 6560–50–P
FOR FURTHER INFORMATION CONTACT:
FEDERAL COMMUNICATIONS
COMMISSION
[OMB 3060–0936]
Information Collection Being
Submitted for Review and Approval to
the Office of Management and Budget
Federal Communications
Commission.
ACTION: Notice and request for
comments.
AGENCY:
As part of its continuing effort
to reduce paperwork burdens, and as
required by the Paperwork Reduction
Act (PRA) of 1995 (44 U.S.C. 3501–
3520), the Federal Communications
Commission (FCC or Commission)
invites the general public and other
Federal agencies to take this
opportunity to comment on the
following information collections.
Comments are requested concerning:
Whether the proposed collection of
information is necessary for the proper
performance of the functions of the
Commission, including whether the
information shall have practical utility;
the accuracy of the Commission’s
burden estimate; ways to enhance the
quality, utility, and clarity of the
information collected; ways to minimize
the burden of the collection of
information on the respondents,
including the use of automated
collection techniques or other forms of
information technology; and ways to
further reduce the information
collection burden on small business
concerns with fewer than 25 employees.
The FCC may not conduct or sponsor a
collection of information unless it
displays a currently valid OMB control
number. No person shall be subject to
any penalty for failing to comply with
a collection of information subject to the
PRA that does not display a valid OMB
control number.
DATES: Written PRA comments should
be submitted on or before September 19,
2016. If you anticipate that you will be
submitting comments, but find it
difficult to do so within the period of
time allowed by this notice, you should
advise the contact listed below as soon
as possible.
ADDRESSES: Direct all PRA comments
Nicholas A. Fraser, OMB, via email:
Nicholas_A._Fraser@omb.eop.gov; and
to Cathy Williams, FCC, via email PRA@
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SUMMARY:
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Federal Communications Commission.
Marlene H. Dortch,
Secretary, Office of the Secretary.
[FR Doc. 2016–19741 Filed 8–17–16; 8:45 am]
BILLING CODE 6712–01–P
For
additional information about the
information collection, contact Cathy
Williams at (202) 418–2918.
SUPPLEMENTARY INFORMATION:
OMB Control No.: 3060–0936.
Title: Sections 95.1215, 95.1217,
95.1223 and 95.1225, Medical Device
Radiocommunications Service
(MedRadio).
Form No.: N/A.
Type of Review: Extension of a
currently approved collection.
Respondents: Business or other forprofit and not-for-profit institutions.
Number of Respondents: 3,120
respondents; 3,120 responses.
Estimated Time per Response: 1–3
hours.
Frequency of Response: On occasion
reporting requirement, third party
disclosure requirement and
recordkeeping requirement.
Obligation to Respond: Required to
obtain or retain benefits. Statutory
authority for this information collection
is contained in 47 U.S.C. 151 and 303
of the Communications Act of 1934, as
amended.
Total Annual Burden: 9,120 hours.
Total Annual Cost: No cost.
Privacy Act Impact Assessment: No
impact(s).
Nature and Extent of Confidentiality:
There is no need for confidentiality with
this collection of information.
Needs and Uses: The Federal
Communications Commission is
requesting that the Office of
Management and Budget (OMB)
approve for a period of three years an
extension for the information collection
requirements contained in this
collection.
The information collection
requirements that are approved under
this information collection are
contained in 47 CFR 95.1225(b) and (c),
95.1217(a)(3) and (c), 95.1223 and
95.1225 which relate to the Medical
Device Radiocommunication Service
(MedRadio).
The information is necessary to allow
the coordinator and parties using the
database to contact other users to verify
information and resolve potential
conflicts. Each user is responsible for
determining in advance whether new
devices are likely to cause or be
susceptible to interference from devices
already registered in the coordination
database.
PO 00000
55199
FEDERAL COMMUNICATIONS
COMMISSION
[DA 16–720]
Order Declares JuBe Communications,
LLC’s International Section 214
Authorization Terminated
Federal Communications
Commission.
ACTION: Notice.
AGENCY:
In this document, the
International Bureau of the Federal
Communications Commission
(Commission) declares the international
Section 214 authorization granted to
JuBe Communications, LLC (JuBe)
terminated given JuBe’s inability to
comply with the express condition for
holding the authorization. It also
concludes that JuBe failed to comply
with those requirements of the
Communications Act of 1934, as
amended (the Act) and the
Commission’s rules that ensure that the
Commission can contact and
communicate with the authorization
holder and verify JuBe is still providing
service, which failures have prevented
any way of addressing JuBe’s inability to
comply with the condition of its
authorization.
FOR FURTHER INFORMATION CONTACT: Cara
Grayer, Telecommunications and
Analysis Division, International Bureau
at (202) 418–2960 or Cara.Grayer@
fcc.gov.
SUPPLEMENTARY INFORMATION: This is a
summary of the Commission’s Order,
DA 16–720, adopted and released July 1,
2016.
SUMMARY:
Background
Section 214(a) of the Act prohibits
any carrier from constructing,
extending, acquiring, or operating any
line, and from engaging in transmission
through any such line, without first
obtaining a certificate of authorization
from the Commission. Under Section
214(c) of the Act, the Commission ‘‘may
attach to the issuance of the certificate
such terms and conditions as in its
judgment the public convenience and
necessity may require.’’ On July 27,
2007, the International Bureau granted
JuBe an international Section 214
authorization to provide global or
limited global facility-based service and
global or limited global resale service in
E:\FR\FM\18AUN1.SGM
18AUN1
Agencies
[Federal Register Volume 81, Number 160 (Thursday, August 18, 2016)]
[Notices]
[Page 55199]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-19741]
=======================================================================
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FEDERAL COMMUNICATIONS COMMISSION
[OMB 3060-0936]
Information Collection Being Submitted for Review and Approval to
the Office of Management and Budget
AGENCY: Federal Communications Commission.
ACTION: Notice and request for comments.
-----------------------------------------------------------------------
SUMMARY: As part of its continuing effort to reduce paperwork burdens,
and as required by the Paperwork Reduction Act (PRA) of 1995 (44 U.S.C.
3501-3520), the Federal Communications Commission (FCC or Commission)
invites the general public and other Federal agencies to take this
opportunity to comment on the following information collections.
Comments are requested concerning: Whether the proposed collection of
information is necessary for the proper performance of the functions of
the Commission, including whether the information shall have practical
utility; the accuracy of the Commission's burden estimate; ways to
enhance the quality, utility, and clarity of the information collected;
ways to minimize the burden of the collection of information on the
respondents, including the use of automated collection techniques or
other forms of information technology; and ways to further reduce the
information collection burden on small business concerns with fewer
than 25 employees. The FCC may not conduct or sponsor a collection of
information unless it displays a currently valid OMB control number. No
person shall be subject to any penalty for failing to comply with a
collection of information subject to the PRA that does not display a
valid OMB control number.
DATES: Written PRA comments should be submitted on or before September
19, 2016. If you anticipate that you will be submitting comments, but
find it difficult to do so within the period of time allowed by this
notice, you should advise the contact listed below as soon as possible.
ADDRESSES: Direct all PRA comments Nicholas A. Fraser, OMB, via email:
Nicholas_A._Fraser@omb.eop.gov; and to Cathy Williams, FCC, via email
PRA@fcc.gov and to Cathy.Williams@fcc.gov. Include in the comments the
OMB control number as shown in the SUPPLEMENTARY INFORMATION section
below.
FOR FURTHER INFORMATION CONTACT: For additional information about the
information collection, contact Cathy Williams at (202) 418-2918.
SUPPLEMENTARY INFORMATION:
OMB Control No.: 3060-0936.
Title: Sections 95.1215, 95.1217, 95.1223 and 95.1225, Medical
Device Radiocommunications Service (MedRadio).
Form No.: N/A.
Type of Review: Extension of a currently approved collection.
Respondents: Business or other for-profit and not-for-profit
institutions.
Number of Respondents: 3,120 respondents; 3,120 responses.
Estimated Time per Response: 1-3 hours.
Frequency of Response: On occasion reporting requirement, third
party disclosure requirement and recordkeeping requirement.
Obligation to Respond: Required to obtain or retain benefits.
Statutory authority for this information collection is contained in 47
U.S.C. 151 and 303 of the Communications Act of 1934, as amended.
Total Annual Burden: 9,120 hours.
Total Annual Cost: No cost.
Privacy Act Impact Assessment: No impact(s).
Nature and Extent of Confidentiality: There is no need for
confidentiality with this collection of information.
Needs and Uses: The Federal Communications Commission is requesting
that the Office of Management and Budget (OMB) approve for a period of
three years an extension for the information collection requirements
contained in this collection.
The information collection requirements that are approved under
this information collection are contained in 47 CFR 95.1225(b) and (c),
95.1217(a)(3) and (c), 95.1223 and 95.1225 which relate to the Medical
Device Radiocommunication Service (MedRadio).
The information is necessary to allow the coordinator and parties
using the database to contact other users to verify information and
resolve potential conflicts. Each user is responsible for determining
in advance whether new devices are likely to cause or be susceptible to
interference from devices already registered in the coordination
database.
Federal Communications Commission.
Marlene H. Dortch,
Secretary, Office of the Secretary.
[FR Doc. 2016-19741 Filed 8-17-16; 8:45 am]
BILLING CODE 6712-01-P