THYRO-INDICATOR T-3 125I— 510(k) K780018

Substantially Equivalent

Clinical Immuno-Diagnostics

FDA 510(k) clearance K780018 for THYRO-INDICATOR T-3 125I, Substantially Equivalent on 1978-02-07. Applicant: Clinical Immuno-Diagnostics.

Clearance details

Applicant: Clinical Immuno-Diagnostics
Product code: Code CDP
Advisory panel: Clinical Chemistry
Date received: 1978-01-03
Decision date: 1978-02-07
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.