FDA 510(k)

TRIIODOTHYRONINE RIA SYSTEM

K-Number: K792539 · 1980-01-16

Decision Date1980-01-16

Product CodeCDP

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

TRIIODOTHYRONINE RIA SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Radioimmunoassay, Inc.. It received FDA 510(k) clearance on 1980-01-16 under 510(k) number K792539. The device is classified under product code CDP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIIODOTHYRONINE RIA SYSTEM?

TRIIODOTHYRONINE RIA SYSTEM is a medical device that received FDA 510(k) clearance on 1980-01-16. The listed applicant is Radioimmunoassay, Inc.. The 510(k) number is K792539.

When did TRIIODOTHYRONINE RIA SYSTEM receive FDA 510(k) clearance?

TRIIODOTHYRONINE RIA SYSTEM received FDA 510(k) clearance on 1980-01-16, under 510(k) number K792539.

Who is the listed applicant for TRIIODOTHYRONINE RIA SYSTEM?

The FDA 510(k) record lists Radioimmunoassay, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRIIODOTHYRONINE RIA SYSTEM?

The FDA product code for TRIIODOTHYRONINE RIA SYSTEM is CDP.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.