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CDRH Appeals Processes Guidance Document
Guidance for Center for Devices and Radiological Health Appeals Processes
OMB: 0910-0738
IC ID: 206202
OMB.report
HHS/FDA
OMB 0910-0738
ICR 201604-0910-002
IC 206202
( )
⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0738 can be found here:
2022-08-24 - Revision of a currently approved collection
2019-07-24 - Extension without change of a currently approved collection
Documents and Forms
Document Name
Document Type
0738_Guidance.pdf
Guidance
IC Document
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 10.75
Information Collection Instruments:
Document Type
Form No.
Form Name
Instrument File
URL
Available Electronically?
Can Be Submitted Electronically?
Electronic Capability
Federal Enterprise Architecture Business Reference Module
Line of Business:
Health
Subfunction:
Immunization Management
Privacy Act System of Records
Title:
FR Citation:
Number of Respondents:
50
Number of Respondents for Small Entity:
0
Affected Public:
Private Sector
Private Sector:
Businesses or other for-profits
Percentage of Respondents Reporting Electronically:
70 %
Approved
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
50
0
0
0
0
50
Annual IC Time Burden (Hours)
400
0
0
0
0
400
Annual IC Cost Burden (Dollars)
0
0
0
0
0
0
Documents for IC
Title
Document
Date Uploaded
Guidance
0738_Guidance.pdf
04/15/2016
Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.