T-3 RIASSAY— 510(k) K852537

Substantially Equivalent

Ria Diagnostics

FDA 510(k) clearance K852537 for T-3 RIASSAY, Substantially Equivalent on 1985-08-12. Applicant: Ria Diagnostics.

Clearance details

Applicant: Ria Diagnostics
Product code: Code CDP
Advisory panel: Clinical Chemistry
Date received: 1985-06-14
Decision date: 1985-08-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Fe Springs, CA, 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.