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FDA 510(k)

VITEK 2 AST-YS Caspofungin <=0.125 - >=8 ug/mL

K-Number: K151817 · 2016-02-18

ApplicantbioMerieux, Inc.
Decision Date2016-02-18
Product CodeNGZ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

VITEK 2 AST-YS Caspofungin <=0.125 - >=8 ug/mL is a medical device manufactured by bioMerieux, Inc.. It received FDA 510(k) clearance on 2016-02-18 under approval number K151817. 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-YS Caspofungin <=0.125 - >=8 ug/mL?

VITEK 2 AST-YS Caspofungin <=0.125 - >=8 ug/mL is a medical device that received FDA 510(k) clearance on 2016-02-18. It is manufactured by bioMerieux, Inc.. The 510(k) number is K151817.

When was VITEK 2 AST-YS Caspofungin <=0.125 - >=8 ug/mL approved by the FDA?

VITEK 2 AST-YS Caspofungin <=0.125 - >=8 ug/mL received FDA 510(k) clearance on 2016-02-18, under approval number K151817.

What company makes VITEK 2 AST-YS Caspofungin <=0.125 - >=8 ug/mL?

VITEK 2 AST-YS Caspofungin <=0.125 - >=8 ug/mL is manufactured by bioMerieux, Inc..

What is the FDA product code for VITEK 2 AST-YS Caspofungin <=0.125 - >=8 ug/mL?

The FDA product code for VITEK 2 AST-YS Caspofungin <=0.125 - >=8 ug/mL is NGZ.

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Related Devices (Code: NGZ)

K151923VITEK 2 AST-Yeast Micafungin (0.06-8 mcg/mL)bioMerieux, Inc. K181368VITEK 2 AST-YS Micafungin (<=0.06 - =>8 µg/mL)bioMerieux, Inc. K211539Sensititre YeastOne Susceptibility System with Voriconazole in the dilution range of 0.008 - 8 ug/mLThermo Fisher Scientific K231433The Sensititre YeastOne Susceptibility System with Rezafungin in the dilution range of 0.008-8ug/mLThermo Fisher Scientific K221198Sensititre YeastOne Susceptibility System with Fluconazole in the dilution range of 0.12-128ug/mLThermo Fisher Scientific K221899The Sensititre YeastOne Susceptibility System with Caspofungin in the dilution range of 0.015-16ug/mlThermo Fisher Scientific

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.

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