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 a medical device manufactured by bioMerieux, Inc.. It received FDA 510(k) clearance on 2022-10-13 under approval 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. It is manufactured by bioMerieux, Inc.. The 510(k) number is K220805.

When was VITEK 2 AST-Gram Positive Cefoxitin Screen approved by the FDA?

VITEK 2 AST-Gram Positive Cefoxitin Screen received FDA 510(k) clearance on 2022-10-13, under approval number K220805.

What company makes VITEK 2 AST-Gram Positive Cefoxitin Screen?

VITEK 2 AST-Gram Positive Cefoxitin Screen is manufactured by bioMerieux, Inc..

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.

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Other Devices by bioMerieux, Inc.

K162076chromID MRSA K161227VITEK 2 AST-GN Cefepime (<=0.12->=32 ug/mL) K160911VIDAS B.R.A.H.M.S. PCT (PCT) K152075VITEK 2 AST-Gram Negative Ertapenem (<=0.12 - >=8 ug/mL) K151923VITEK 2 AST-Yeast Micafungin (0.06-8 mcg/mL) K151688chromID MRSA

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Related Devices (Code: LON)

K161227VITEK 2 AST-GN Cefepime (<=0.12->=32 ug/mL)bioMerieux, Inc. K152075VITEK 2 AST-Gram Negative Ertapenem (<=0.12 - >=8 ug/mL)bioMerieux, Inc. K151320BD Phoenix Automated Microbiology System-Ertapenem 0.0625-8 mcg/mlBecton, Dickinson and Company K172944VITEK 2 AST-GN Ceftazidime/Avibactam <=0.12 >=16 µg/mLbioMerieux, Inc. K172731VITEK 2 AST-GN Amikacin (<=1 ->=64 ug/mL)bioMerieux, Inc. K162737VITEK 2 AST-GN Ciprofloxacin (<=0.06->=4µg/mL)bioMerieux, Inc.

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.