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FDA 510(k)

VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL)

K-Number: K232963 · 2024-06-07

Decision Date2024-06-07
Product CodeNGZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL) is a medical device manufactured by bioMerieux, Inc.. It received FDA 510(k) clearance on 2024-06-07 under approval number K232963. The device is classified under product code NGZ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL)?

VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL) is a medical device that received FDA 510(k) clearance on 2024-06-07. It is manufactured by bioMerieux, Inc.. The 510(k) number is K232963.

When was VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL) approved by the FDA?

VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL) received FDA 510(k) clearance on 2024-06-07, under approval number K232963.

What company makes VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL)?

VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL) is manufactured by bioMerieux, Inc..

What is the FDA product code for VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL)?

The FDA product code for VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL) is NGZ.

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Official Source

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