VTEK 2 AST-GN Ceftolozane/Tazobactam (<=0.25 - >= 32 mcg/mL)
K-Number: K161510 · 2017-02-13
Device Summary
Frequently Asked Questions
What is the VTEK 2 AST-GN Ceftolozane/Tazobactam (<=0.25 - >= 32 mcg/mL)?
VTEK 2 AST-GN Ceftolozane/Tazobactam (<=0.25 - >= 32 mcg/mL) is a medical device that received FDA 510(k) clearance on 2017-02-13. It is manufactured by bioMerieux, Inc.. The 510(k) number is K161510.
When was VTEK 2 AST-GN Ceftolozane/Tazobactam (<=0.25 - >= 32 mcg/mL) approved by the FDA?
VTEK 2 AST-GN Ceftolozane/Tazobactam (<=0.25 - >= 32 mcg/mL) received FDA 510(k) clearance on 2017-02-13, under approval number K161510.
What company makes VTEK 2 AST-GN Ceftolozane/Tazobactam (<=0.25 - >= 32 mcg/mL)?
VTEK 2 AST-GN Ceftolozane/Tazobactam (<=0.25 - >= 32 mcg/mL) is manufactured by bioMerieux, Inc..
What is the FDA product code for VTEK 2 AST-GN Ceftolozane/Tazobactam (<=0.25 - >= 32 mcg/mL)?
The FDA product code for VTEK 2 AST-GN Ceftolozane/Tazobactam (<=0.25 - >= 32 mcg/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.