T3 RIA— 510(k) K771623

Substantially Equivalent

Hoffmann-La Roche, Inc.

FDA 510(k) clearance K771623 for T3 RIA, Substantially Equivalent on 1977-09-20. Applicant: Hoffmann-La Roche, Inc..

Clearance details

Applicant: Hoffmann-La Roche, Inc.
Product code: Code CDP
Advisory panel: Clinical Chemistry
Date received: 1977-08-25
Decision date: 1977-09-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.