Form 3673 Device Registration & Listing Module

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

Form FDA 3673 Device Regs & Liasting Module

Reporting- Annual Registration Requirements Each Fiscal Year For All Establishments

OMB: 0910-0625

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Device Registration and Listing Module


Form Number: FDA 3673


OMB Number: 0910- 0625


OMB Expiration Date: 03/31/2012


OMB Burden Statement:


Public reporting burden for this collection of information on Form 3673 is estimated to be 0.50 hours per response for the purpose of firms annually registering their establishment and 0.25 hours per response for the purpose of firms annually listing their devices. These estimates are based on FDA's experience, data from the device registration and listing database, and our estimates of the time needed to complete other previously required forms.

Send comments regarding this burden estimate or another aspect of this collection of information, including suggestions for reducing this burden to:

Department of Health and Human Services

Food and Drug Administration

Office of the Chief Information Officer

1350 Piccard Dr.
Rockville, Maryland 20850

An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid Office of Management and Budget (OMB) control number.




File Typeapplication/msword
AuthorDavid Racine
Last Modified ByDPresley
File Modified2010-05-12
File Created2010-05-12

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