VITEK 2 AST-Gram Negative Fosfomycin (<=4 - >=256 µg/mL), VITEK 2 AST-GN Fosfomycin (<=4 - >=256 µg/mL), VITEK 2 AST-GN Fosfomycin— 510(k) K222430

Substantially Equivalent

Biomerieux Sa, Inc.

FDA 510(k) clearance K222430 for VITEK 2 AST-Gram Negative Fosfomycin (<=4 - >=256 µg/mL), VITEK 2 AST-GN Fosfomycin (<=4 - >=256 µg/mL), VITEK 2 AST-GN Fosfomycin, Substantially Equivalent on 2023-03-09. Applicant: Biomerieux Sa, Inc..

Clearance details

Applicant: Biomerieux Sa, Inc.
Product code: Code LON
Advisory panel: Microbiology
Date received: 2022-08-11
Decision date: 2023-03-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hazelwood, MO, US

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Adverse events under product code LON

product code LON

Malfunction: 2,383
Total: 2,383

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.