VIDAS TOXO IGG AVIDITY— 510(k) K101946

Substantially Equivalent

bioMerieux, Inc.

FDA 510(k) clearance K101946 for VIDAS TOXO IGG AVIDITY, Substantially Equivalent on 2011-05-18. Applicant: bioMerieux, Inc..

Clearance details

Applicant: bioMerieux, Inc.
Product code: Code LGD
Advisory panel: Microbiology
Date received: 2010-07-12
Decision date: 2011-05-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hazelwood, MO, US

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Adverse events under product code LGD

product code LGD

Malfunction: 502
Total: 502

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.