VITEK 2 AST-YS Micafungin (<=0.06 - =>8 µg/mL)
K-Number: K181368 · 2018-06-20
Device Summary
Frequently Asked Questions
What is the VITEK 2 AST-YS Micafungin (<=0.06 - =>8 µg/mL)?
VITEK 2 AST-YS Micafungin (<=0.06 - =>8 µg/mL) is a medical device that received FDA 510(k) clearance on 2018-06-20. It is manufactured by bioMerieux, Inc.. The 510(k) number is K181368.
When was VITEK 2 AST-YS Micafungin (<=0.06 - =>8 µg/mL) approved by the FDA?
VITEK 2 AST-YS Micafungin (<=0.06 - =>8 µg/mL) received FDA 510(k) clearance on 2018-06-20, under approval number K181368.
What company makes VITEK 2 AST-YS Micafungin (<=0.06 - =>8 µg/mL)?
VITEK 2 AST-YS Micafungin (<=0.06 - =>8 µg/mL) is manufactured by bioMerieux, Inc..
What is the FDA product code for VITEK 2 AST-YS Micafungin (<=0.06 - =>8 µg/mL)?
The FDA product code for VITEK 2 AST-YS Micafungin (<=0.06 - =>8 µg/mL) is NGZ.
Other Devices by bioMerieux, Inc.
Related Devices (Code: NGZ)
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.