Reporting - Initial Registration & Listing Information ( to be sent by letter) For Owners / Operators Granted a Waiver From Electronic Filing ( one time burden)

Implementation of Sections 222, 223 and 224 of the Food and Drug Administration Act of 2007

OMB: 0910-0625

IC ID: 193009

Information Collection (IC) Details

View Information Collection (IC)

Reporting - Initial Registration & Listing Information ( to be sent by letter) For Owners / Operators Granted a Waiver From Electronic Filing ( one time burden)
 
No New
 
Mandatory
 
21 CFR 807.34 (a)

Document Type Form No. Form Name Instrument File URL Available Electronically? Can Be Submitted Electronically? Electronic Capability
Form and Instruction 3673 Device Registration & Listing Module Form FDA 3673 Device Regs & Liasting Module.doc Yes Yes Fillable Fileable

Health Consumer Health and Safety

 

20 0
   
Private Sector Businesses or other for-profits
 
   0 %

  Requested 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 20 0 0 0 0
Annual IC Time Burden (Hours) 20 20 0 0 0 0
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