VITEK ANAEROBE IDENTIFICATION CARD— 510(k) K900996

Name: FDA 510(k) clearance K900996
Creator: U.S. Food and Drug Administration
Published: 1990-05-11

Substantially Equivalent

Vitek Systems, Inc.

FDA 510(k) clearance K900996 for VITEK ANAEROBE IDENTIFICATION CARD, Substantially Equivalent on 1990-05-11. Applicant: Vitek Systems, Inc.. Device class: 1.

Clearance details

Applicant: Vitek Systems, Inc.
Product code: Code JSP
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1990-03-02
Decision date: 1990-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hazelwood, MI, US

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