Medical Device Recall Authority

Medical Device Recall Authority

OMB: 0910-0432

IC ID: 6106

Documents and Forms
Document Name
Document Type
no available documents/forms check other ICs listed under this ICR
Information Collection (IC) Details

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Medical Device Recall Authority
 
No Modified
 
Mandatory
 
21 CFR 810.10(d) 21 CFR 810.11(a) 21 CFR 810.12 (a-b) 21 CFR 810.14 21 CFR 810.15 (a-c) 21 CFR 810.15(d) 21 CFR 810.15 (e) 21 CFR 810.16 (a-b) 21 CFR 810.17 ( a) 21 CFR 810.15 (b)

Document Type Form No. Form Name Instrument File URL Available Electronically? Can Be Submitted Electronically? Electronic Capability

Health Consumer Health and Safety

 

2 0
   
Private Sector Businesses or other for-profits
 
   0 %

  Approved Program Change Due to New Statute Program Change Due to Agency Discretion Change Due to Adjustment in Agency Estimate Change Due to Potential Violation of the PRA Previously Approved
Annual Number of Responses for this IC 2 0 0 0 0 2
Annual IC Time Burden (Hours) 1,090 0 0 8 0 1,082
Annual IC Cost Burden (Dollars) 0 0 0 0 0 0

Title Document Date Uploaded
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            Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.

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