VITEK 2 AST-Streptococcus Cefuroxime (<=0.125 - >=8 µg/mL)
K-Number: K260281 · 2026-03-26
Device Summary
Frequently Asked Questions
What is the VITEK 2 AST-Streptococcus Cefuroxime (<=0.125 - >=8 µg/mL)?
VITEK 2 AST-Streptococcus Cefuroxime (<=0.125 - >=8 µg/mL) is a medical device that received FDA 510(k) clearance on 2026-03-26. It is manufactured by BIOMERIEUX. The 510(k) number is K260281.
When was VITEK 2 AST-Streptococcus Cefuroxime (<=0.125 - >=8 µg/mL) approved by the FDA?
VITEK 2 AST-Streptococcus Cefuroxime (<=0.125 - >=8 µg/mL) received FDA 510(k) clearance on 2026-03-26, under approval number K260281.
What company makes VITEK 2 AST-Streptococcus Cefuroxime (<=0.125 - >=8 µg/mL)?
VITEK 2 AST-Streptococcus Cefuroxime (<=0.125 - >=8 µg/mL) is manufactured by BIOMERIEUX.
What is the FDA product code for VITEK 2 AST-Streptococcus Cefuroxime (<=0.125 - >=8 µg/mL)?
The FDA product code for VITEK 2 AST-Streptococcus Cefuroxime (<=0.125 - >=8 µg/mL) is LON.
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.