VITEK 2 AST-Gram Positive Lefamulin (<=0.03 - >=4 µg/mL)
K-Number: K234000 · 2024-03-11
Device Summary
Frequently Asked Questions
What is the VITEK 2 AST-Gram Positive Lefamulin (<=0.03 - >=4 µg/mL)?
VITEK 2 AST-Gram Positive Lefamulin (<=0.03 - >=4 µg/mL) is a medical device that received FDA 510(k) clearance on 2024-03-11. It is manufactured by bioMerieux, Inc.. The 510(k) number is K234000.
When was VITEK 2 AST-Gram Positive Lefamulin (<=0.03 - >=4 µg/mL) approved by the FDA?
VITEK 2 AST-Gram Positive Lefamulin (<=0.03 - >=4 µg/mL) received FDA 510(k) clearance on 2024-03-11, under approval number K234000.
What company makes VITEK 2 AST-Gram Positive Lefamulin (<=0.03 - >=4 µg/mL)?
VITEK 2 AST-Gram Positive Lefamulin (<=0.03 - >=4 µg/mL) is manufactured by bioMerieux, Inc..
What is the FDA product code for VITEK 2 AST-Gram Positive Lefamulin (<=0.03 - >=4 µg/mL)?
The FDA product code for VITEK 2 AST-Gram Positive Lefamulin (<=0.03 - >=4 µg/mL) is LON.
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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.