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U.S. Department of Health and Human Services

FDA Application

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Federal Register
Tuesday November 8, 2011

Planning to Submit Comments?

Documents and comments received by the Division of Dockets Management may be posted on the Internet. Please do not include personal identifying information, i.e. date of birth, social security number, medical information, etc., in your correspondence.
Submit Electronic Comments

Documents are on display for public inspection at the Division of Dockets Management, 5630 Fishers Lane (Room 1061), HFA-305, Rockville, MD, 20852; 301-827-6860; TTY/TDD Users 1-800-735-2258.


FDA Federal Register Documents

NOTICES

Docket No. FDA-2011-N-0444, ORA 201131.  Gayle Rothenberg: Debarment Order.  Pages  69272-69273 [FR Doc. 2011-28877]  [OFR PUB]

Docket No. FDA-2011-D-0453, CDRH 2011119.  Guidance for Industry and Food and Drug Administration Staff; 510(k) Device Modifications: Deciding When to Submit a 510 (k) for a Change to an Existing Device; Availability; Reopening of Comment Period.  Page  69274 [FR Doc. 2011-28875]  [OFR PUB] Comments due November 28, 2011


Table of Contents for Entire Federal Register
Tuesday, November 8, 2011 [Not Available]

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