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FDA 510(k)

VITEK 2 AST-Gram Positive Cefoxitin Screen

K-Number: K220805 · 2022-10-13

Decision Date2022-10-13
Product CodeLON
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

VITEK 2 AST-Gram Positive Cefoxitin Screen is the device name listed in this FDA 510(k) record. The listed applicant is bioMerieux, Inc.. It received FDA 510(k) clearance on 2022-10-13 under 510(k) number K220805. The device is classified under product code LON. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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.

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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

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