Information Collection

Registration & listing of devices: REPORTING

IC 184861 under ICR 202505-0910-006 · OMB 0910-0625.

Documents and Forms

Documents and forms in this information collection
Document Name	Document Type
Form FDA 3673 Registration & listing of devices: REPORTING	Form
Form FDA 3673 FDA 3673 Registration & listing of devices: REPORTING	Form
FDA 3673 FDA 3673 0625_Form FDA 3673 Screen shots.pdf	Form
FDA 3673 FDA 3673 0625_Form FDA 3673 Screen shots.pdf	Form

IC Title:

Agency IC Tracking Number:

Is this a Common Form? No

IC Status: Modified

Obligation to Respond: Mandatory

CFR Citation: 21 CFR 807

Information Collection Instruments:

table that charts list of instruments
Document Type	Form No.	Form Name	Instrument File	URL	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Form	FDA 3673				Yes	Yes	Fillable Fileable Signable

Line of Business: Health

Subfunction: Consumer Health and Safety

Privacy Act System of Records

Title:

FR Citation:

Number of Respondents: 95,781

Number of Respondents for Small Entity: 0

Affected Public: Private Sector

Private Sector: Businesses or other for-profits

Percentage of Respondents Reporting Electronically: 99 %

table that charts list of burden
	Approved	Change Due to Adjustment in Agency Estimate	Previously Approved
Annual Number of Responses for this IC	106,309	-12,485	118,794
Annual IC Time Burden (Hours)	55,641	-15,662	71,303
Annual IC Cost Burden (Dollars)	0	0	0

Documents for IC

table that charts IC Documents
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.

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