VITEK 2 AST-Gram Negative Meropenem/Vaborbactam (<=0.5/8 >=64/8 µg/mL)— 510(k) K183360

Substantially Equivalent

bioMerieux, Inc.

FDA 510(k) clearance K183360 for VITEK 2 AST-Gram Negative Meropenem/Vaborbactam (<=0.5/8 >=64/8 µg/mL), Substantially Equivalent on 2019-02-26. Applicant: bioMerieux, Inc..

Clearance details

Applicant: bioMerieux, Inc.
Product code: Code LON
Advisory panel: Microbiology
Date received: 2018-12-04
Decision date: 2019-02-26
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.