Medical Device Manufacturer · US , Hazelwood , MO

Biomerieux Sa, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2023

Recent clearances: VITEK 2 AST-Gram Negative Fosfomycin (<=4 - >=256 µg/mL), VITEK 2 AST-GN Fosfomycin (<=4 - >=256 µg/mL), VITEK 2 AST-GN Fosfomycin

1
Total
1
Cleared
0
Denied

Biomerieux Sa, Inc. has 1 FDA 510(k) cleared medical devices. Based in Hazelwood, US.

Last cleared in 2023. Active since 2023. Primary specialty: Microbiology.

Browse the FDA 510(k) cleared devices submitted by Biomerieux Sa, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Biomerieux Sa, Inc.

1 devices
1-1 of 1
Cleared Mar 09, 2023
VITEK 2 AST-Gram Negative Fosfomycin (<=4 - >=256 µg/mL), VITEK 2 AST-GN...
K222430 · LON
Microbiology · 210d
Filters
Filter by Specialty
All1 Microbiology 1