GIBSON ID A.E. TEST— 510(k) K953247

Substantially Equivalent

Gibson Laboratories, Inc.

FDA 510(k) clearance K953247 for GIBSON ID A.E. TEST, Substantially Equivalent on 1995-11-20. Applicant: Gibson Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Gibson Laboratories, Inc.
Product code: Code JTO
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1995-07-11
Decision date: 1995-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lexington, KY, US

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