MODEL UCG ASSAY— 510(k) K822520

Substantially Equivalent

Monoclonal Antibodies, Inc.

FDA 510(k) clearance K822520 for MODEL UCG ASSAY, Substantially Equivalent on 1982-09-28. Applicant: Monoclonal Antibodies, Inc..

Clearance details

Applicant: Monoclonal Antibodies, Inc.
Product code: Code JHI
Advisory panel: Clinical Chemistry
Date received: 1982-08-23
Decision date: 1982-09-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code JHI

product code JHI

Malfunction: 1,055
Total: 1,055

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.