HCG SEROZYME IMMUNOENZYM ASSAY KIT/MAG SOLID PHASE— 510(k) K873033

Substantially Equivalent

Serono Diagnostics, Inc.

FDA 510(k) clearance K873033 for HCG SEROZYME IMMUNOENZYM ASSAY KIT/MAG SOLID PHASE, Substantially Equivalent on 1987-09-14. Applicant: Serono Diagnostics, Inc..

Clearance details

Applicant: Serono Diagnostics, Inc.
Product code: Code JHI
Advisory panel: Clinical Chemistry
Date received: 1987-08-04
Decision date: 1987-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwell, MA, 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.