ACCESS TOTAL T3 ASSAY (MODIFICATION)— 510(k) K955435

Substantially Equivalent

Bio-Rad Laboratories, Inc.

FDA 510(k) clearance K955435 for ACCESS TOTAL T3 ASSAY (MODIFICATION), Substantially Equivalent on 1996-01-24. Applicant: Bio-Rad Laboratories, Inc..

Clearance details

Applicant: Bio-Rad Laboratories, Inc.
Product code: Code CDP
Advisory panel: Clinical Chemistry
Date received: 1995-10-02
Decision date: 1996-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chaska, MN, 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.