Recordkeeping Postmarket Surveillance of Medical Devices: manufacturer and investigator records

Postmarket Surveillance of Medical Devices

OMB: 0910-0449

IC ID: 192723

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

View Information Collection (IC)

Recordkeeping Postmarket Surveillance of Medical Devices: manufacturer and investigator records
 
No Modified
 
Mandatory
 
21 CFR 822

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

Health Consumer Health and Safety

 

20 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 20 0 0 -55 0 75
Annual IC Time Burden (Hours) 175 0 0 -700 0 875
Annual IC Cost Burden (Dollars) 0 0 0 0 0 0

Title Document Date Uploaded
No associated records found
            Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.

© 2024 OMB.report | Privacy Policy