CHANGING METHOD OF STERILITY RELEASE— 510(k) K832368

Name: FDA 510(k) clearance K832368
Creator: U.S. Food and Drug Administration
Published: 1983-10-31

Substantially Equivalent

Devon Industries, Inc.

FDA 510(k) clearance K832368 for CHANGING METHOD OF STERILITY RELEASE, Substantially Equivalent on 1983-10-31. Applicant: Devon Industries, Inc.. Device class: 1.

Clearance details

Applicant: Devon Industries, Inc.
Product code: Code EMF
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1983-07-18
Decision date: 1983-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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Data sourced from openFDA. This site is unofficial and independent of the FDA.