Withdrawal of Federal Register Notice

---
identifier: "/us/fr/E6-20705"
source: "fr"
legal_status: "authoritative_unofficial"
title: "Withdrawal of Federal Register Notice"
title_number: 0
title_name: "Federal Register"
section_number: "E6-20705"
section_name: "Withdrawal of Federal Register Notice"
positive_law: false
currency: "2006-12-07"
last_updated: "2006-12-07"
format_version: "1.1.0"
generator: "[email protected]"
agency: "Health and Human Services Department"
document_number: "E6-20705"
document_type: "notice"
publication_date: "2006-12-07"
agencies:
  - "Health and Human Services Department"
  - "Food and Drug Administration"
fr_citation: "71 FR 70973"
fr_volume: 71
docket_ids:
  - "Docket No. 2006N-0426"
fr_action: "Notice; withdrawal."
---


#  Withdrawal of Federal Register Notice

**AGENCY:**

Food and Drug Administration, HHS.

**ACTION:**

Notice; withdrawal.

**SUMMARY:**

The Food and Drug Administration (FDA) is announcing the withdrawal of a 60-day notice that published in the *Federal Register* of October 31, 2006 (71 FR 63765). The document published in error.

**DATES:**

December 7, 2006.

**FOR FURTHER INFORMATION CONTACT:**

Denver Presley, Jr., Office of the Chief Information Officer (HFA-250), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301-827-1472.

**SUPPLEMENTARY INFORMATION:**

FDA is withdrawing a 60-day notice entitled “Medical Device User Fee and Modernization Act Small Business Qualification Certification (Form FDA 3602),” which published in the *Federal Register* of October 31, 2006 (71 FR 63765), because it is a duplicate of an earlier 60-day notice. The earlier 60-day notice published in the *Federal Register* of August 29, 2006 (71 FR 51196). The October 31 notice was published in error.

Dated: November 30, 2006.

Jeffrey Shuren,

Assistant Commissioner for Policy.