VITEK 2 AST-Yeast Anidulafungin (<= 0.015 - >= 8 µg/mL)
K-Number: K232963 · 2024-06-07
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.