T3 SEROZYME ENZYMEIMMUNOASSAY KIT, MAG SOLID PHASE— 510(k) K880388

Substantially Equivalent

Serono Diagnostics, Inc.

FDA 510(k) clearance K880388 for T3 SEROZYME ENZYMEIMMUNOASSAY KIT, MAG SOLID PHASE, Substantially Equivalent on 1988-03-03. Applicant: Serono Diagnostics, Inc..

Clearance details

Applicant: Serono Diagnostics, Inc.
Product code: Code CDP
Advisory panel: Clinical Chemistry
Date received: 1988-01-28
Decision date: 1988-03-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Norwell, MA, US

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Adverse events under product code CDP

product code CDP

Malfunction: 647
Total: 647

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.