Information Collection

CDRH Appeals Processes Guidance Document

IC 206202 under ICR 202508-0910-001 · OMB 0910-0738.

Documents and Forms

Document Name Document Type
0910-0738_Guidance; Center for Devices and Radiological Health (CDRH).pdf www.fda.gov/regulatory-information/search-fda-guidance-documents/center-devices-and-radiological-health-cdrh-appeals-pro Other-Guidance - CDRH Appeals Proces

Information Collection (IC) Details

View Information Collection (IC)

IC Title:	CDRH Appeals Processes Guidance Document	Agency IC Tracking Number:

Is this a Common Form? No		IC Status: Modified

Obligation to Respond: Voluntary

CFR Citation: 21 CFR 10

Information Collection Instruments:

Document Type	Form No.	Form Name	Instrument File	URL	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Other-Guidance - CDRH Appeals Process			0910-0738_Guidance; Center for Devices and Radiological Health (CDRH).pdf	https://www.fda.gov/regulatory-information/search-fda-guidance-documents/center-devices-and-radiological-health-cdrh-appeals-processes	Yes	Yes	Fillable Fileable

Line of Business: Health

Subfunction: Consumer Health and Safety

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 75	Number of Respondents for Small Entity: 0

Affected Public: Private Sector	Private Sector: Businesses or other for-profits

Percentage of Respondents Reporting Electronically: 99 %

	Requested	Change Due to Adjustment in Agency Estimate	Change Due to Potential Violation of the PRA
Annual Number of Responses for this IC	75	40	35
Annual IC Time Burden (Hours)	600	320	280
Annual IC Cost Burden (Dollars)	0	0	0

Documents for IC

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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