VITEK 2 AST-Gram Positive Cefoxitin Screen
K-Number: K220805 · 2022-10-13
Device Summary
Frequently Asked Questions
What is the VITEK 2 AST-Gram Positive Cefoxitin Screen?
VITEK 2 AST-Gram Positive Cefoxitin Screen is a medical device that received FDA 510(k) clearance on 2022-10-13. The listed applicant is bioMerieux, Inc.. The 510(k) number is K220805.
When did VITEK 2 AST-Gram Positive Cefoxitin Screen receive FDA 510(k) clearance?
VITEK 2 AST-Gram Positive Cefoxitin Screen received FDA 510(k) clearance on 2022-10-13, under 510(k) number K220805.
Who is the listed applicant for VITEK 2 AST-Gram Positive Cefoxitin Screen?
The FDA 510(k) record lists bioMerieux, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VITEK 2 AST-Gram Positive Cefoxitin Screen?
The FDA product code for VITEK 2 AST-Gram Positive Cefoxitin Screen is LON.
Other records listing bioMerieux, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LON)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.