Reporting- Fiscal Year Update Requirements For Owners / Operarors to Review / Update Device Listing Information On File With FDA For the Period October 1 and Ending December 31.

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

OMB: 0910-0625

IC ID: 193007

Information Collection (IC) Details

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Reporting- Fiscal Year Update Requirements For Owners / Operarors to Review / Update Device Listing Information On File With FDA For the Period October 1 and Ending December 31.
 
No New
 
Mandatory
 
21 CFR 807.22 (b) (3)

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

 

24,870 0
   
Private Sector Businesses or other for-profits
 
   99 %

  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 24,870 24,870 0 0 0 0
Annual IC Time Burden (Hours) 24,870 24,870 0 0 0 0
Annual IC Cost Burden (Dollars) 0 0 0 0 0 0

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