Health Care Practitioners' Responses to Medical Device Labeling

Focus Groups as Used by the Food and Drug Administration

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0497 can be found here:

Documents and Forms

Document Name Document Type
Consent for Participation.doc Instruction
Moderator's Guide.doc Instruction
Questionnaire.doc Instruction
Screening Script.doc Instruction
Topics for Labeling.doc Instruction
OMB Justification Memo.doc OMB Justification Memo IC Document

Information Collection (IC) Details

IC Title:	Health Care Practitioners' Responses to Medical Device Labeling	Agency IC Tracking Number:

IC Status: New

Obligation to Respond: Voluntary

CFR Citation:

Information Collection Instruments:

Document Type	Instrument File	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Instruction	Consent for Participation.doc	No	No	Paper Only
Instruction	Moderator's Guide.doc	No	No	Paper Only
Instruction	Questionnaire.doc	No	No	Paper Only
Instruction	Screening Script.doc	No	No	Paper Only
Instruction	Topics for Labeling.doc	No	No	Paper Only

Line of Business: Health

Subfunction: Public Health Monitoring

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 81	Number of Respondents for Small Entity: 0

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

Percentage of Respondents Reporting Electronically: 0 %

	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	81	0	0	0	0	0
Annual IC Time Burden (Hours)	122	0	0	0	0	0
Annual IC Cost Burden (Dollars)	0	0	0	0	0	0

Documents for IC

Title	Document	Date Uploaded
OMB Justification Memo	OMB Justification Memo.doc	12/01/2010

Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.