Biomerieux Sa, Inc.
Biomerieux Sa, Inc. appears in FDA public data with 0 recalls, 1 510(k) clearance, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 9, 2023.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 0
- Compliance Actions
- 0
Known Names
biomerieux, biomerieux vitek, biomerieux italia, biomerieux colombia, biomerieux sa
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K222430 | VITEK 2 AST-Gram Negative Fosfomycin (<=4 - >=256 µg/mL), VITEK 2 AST-GN Fosfomycin (<=4 - >=256 µg/ | March 9, 2023 |