Sections 95.2593, 95.2595 and 95.2509 Medical Device Radiocommunication Service (MedRadio)

ICR 202208-3060-016

OMB: 3060-0936

Federal Form Document

Forms and Documents
Document
Name
Status
Supporting Statement A
2022-08-30
IC Document Collections
ICR Details
3060-0936 202208-3060-016
Received in OIRA 202204-3060-019
FCC WTB
Sections 95.2593, 95.2595 and 95.2509 Medical Device Radiocommunication Service (MedRadio)
Extension without change of a currently approved collection   No
Regular 08/30/2022
  Requested Previously Approved
36 Months From Approved 09/30/2022
3,120 3,120
9,120 9,120
0 0

The information collection requires manufacturers of transmitters for the Medical Device Radiocommunication Service (MedRadio) to include with each transmitting device a statement regarding harmful interference and to label the device in a conspicuous location on the device. It also requires the manufacturers to register the frequencies with the "Database Coordinator. The requirements will allow use of potential life-saving medical technology without causing interference to other users of the bands.

US Code: 47 USC 154, 303 Name of Law: Communications Act of 1934, as amended
  
None

Not associated with rulemaking

  87 FR 37511 06/23/2022
87 FR 52972 08/30/2022
No

1
IC Title Form No. Form Name
Sections 95.2593, 95.2595 and 95.2509 Medical Device Radiocommunication Service (MedRadio)

  Total Request Previously Approved Change Due to New Statute Change Due to Agency Discretion Change Due to Adjustment in Estimate Change Due to Potential Violation of the PRA
Annual Number of Responses 3,120 3,120 0 0 0 0
Annual Time Burden (Hours) 9,120 9,120 0 0 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
No
No

$0
No
    No
    No
No
No
No
No
Jeff Tobias 202 418-0680 [email protected]

  No

On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
 
 
 
 
 
 
 
    (i) Why the information is being collected;
    (ii) Use of information;
    (iii) Burden estimate;
    (iv) Nature of response (voluntary, required for a benefit, or mandatory);
    (v) Nature and extent of confidentiality; and
    (vi) Need to display currently valid OMB control number;
 
 
 
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.
08/30/2022


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