VITEK 2 AST-GN Ceftazidime/Avibactam <=0.12 >=16 µg/mL
K-Number: K172944 · 2017-12-19
Device Summary
Frequently Asked Questions
What is the VITEK 2 AST-GN Ceftazidime/Avibactam <=0.12 >=16 µg/mL?
VITEK 2 AST-GN Ceftazidime/Avibactam <=0.12 >=16 µg/mL is a medical device that received FDA 510(k) clearance on 2017-12-19. It is manufactured by bioMerieux, Inc.. The 510(k) number is K172944.
When was VITEK 2 AST-GN Ceftazidime/Avibactam <=0.12 >=16 µg/mL approved by the FDA?
VITEK 2 AST-GN Ceftazidime/Avibactam <=0.12 >=16 µg/mL received FDA 510(k) clearance on 2017-12-19, under approval number K172944.
What company makes VITEK 2 AST-GN Ceftazidime/Avibactam <=0.12 >=16 µg/mL?
VITEK 2 AST-GN Ceftazidime/Avibactam <=0.12 >=16 µg/mL is manufactured by bioMerieux, Inc..
What is the FDA product code for VITEK 2 AST-GN Ceftazidime/Avibactam <=0.12 >=16 µg/mL?
The FDA product code for VITEK 2 AST-GN Ceftazidime/Avibactam <=0.12 >=16 µg/mL is LON.
Other Devices by bioMerieux, Inc.
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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.