VITEK 2 AST-Gram Negative Ceftazidime (=<0.5 - =>32 µg/mL)
K-Number: K193299 · 2020-09-28
Device Summary
Frequently Asked Questions
What is the VITEK 2 AST-Gram Negative Ceftazidime (=<0.5 - =>32 µg/mL)?
VITEK 2 AST-Gram Negative Ceftazidime (=<0.5 - =>32 µg/mL) is a medical device that received FDA 510(k) clearance on 2020-09-28. It is manufactured by bioMerieux, Inc.. The 510(k) number is K193299.
When was VITEK 2 AST-Gram Negative Ceftazidime (=<0.5 - =>32 µg/mL) approved by the FDA?
VITEK 2 AST-Gram Negative Ceftazidime (=<0.5 - =>32 µg/mL) received FDA 510(k) clearance on 2020-09-28, under approval number K193299.
What company makes VITEK 2 AST-Gram Negative Ceftazidime (=<0.5 - =>32 µg/mL)?
VITEK 2 AST-Gram Negative Ceftazidime (=<0.5 - =>32 µg/mL) is manufactured by bioMerieux, Inc..
What is the FDA product code for VITEK 2 AST-Gram Negative Ceftazidime (=<0.5 - =>32 µg/mL)?
The FDA product code for VITEK 2 AST-Gram Negative Ceftazidime (=<0.5 - =>32 µg/mL) is LON.
Other Devices by bioMerieux, Inc.
Related Devices (Code: LON)
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.