VITEK MS— 510(k) DEN130013

Unknown

bioMerieux, Inc.

FDA 510(k) clearance DEN130013 for VITEK MS, Unknown on 2013-08-21. Applicant: bioMerieux, Inc.. Device class: 2.

Clearance details

Applicant: bioMerieux, Inc.
Product code: Code PEX
Device class: Class 2
Regulation: 21 CFR 866.3361
Advisory panel: Microbiology
Date received: 2013-01-02
Decision date: 2013-08-21
Decision: Unknown
Clearance type: Direct
Location: Hazelwood, MO, US

View on FDA.gov ↗

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