Product Listing Update

Blood Establishment Registration and Product Listing, Form FDA 2830

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0052 can be found here:

Documents and Forms

Document Name Document Type
Form 2830 Product Listing Update Form and Instruction
2830 Blood Establishment Registration and Product Listing FORM FDA 2830 1-21-15.pdf Form and Instruction

Information Collection (IC) Details

IC Title:	Product Listing Update	Agency IC Tracking Number:	CDER

Is this a Common Form? No		IC Status: Modified

Obligation to Respond: Mandatory

CFR Citation: 21 CFR 607.30(a) 21 CFR 607.21 21 CFR 607.31 21 CFR 607.25 21 CFR 607.40

Information Collection Instruments:

Document Type	Form No.	Form Name	Instrument File	URL	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Form and Instruction	2830	Blood Establishment Registration and Product Listing	FORM FDA 2830 1-21-15.pdf		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: 166	Number of Respondents for Small Entity: 0

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

Percentage of Respondents Reporting Electronically: 95 %

	Approved	Change Due to Adjustment in Agency Estimate	Previously Approved
Annual Number of Responses for this IC	166	-14	180
Annual IC Time Burden (Hours)	42	-3	45
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.