Information Collection Being Submitted for Review and Approval to the Office of Management and Budget, 55199 [2016-19741]

Download as PDF 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@ rmajette on DSK2TPTVN1PROD with NOTICES SUMMARY: VerDate Sep<11>2014 15:05 Aug 17, 2016 Jkt 238001 Frm 00030 Fmt 4703 Sfmt 4703 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
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