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FDA 510(k)

TEST, RIA, TRIODOTHYRONINE

K-Number: K760057 · 1976-09-13

ApplicantSmithkline Diagnostics, Inc.
Decision Date1976-09-13
Product CodeCDP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TEST, RIA, TRIODOTHYRONINE is the device name listed in this FDA 510(k) record. The listed applicant is Smithkline Diagnostics, Inc.. It received FDA 510(k) clearance on 1976-09-13 under 510(k) number K760057. 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 TEST, RIA, TRIODOTHYRONINE?

TEST, RIA, TRIODOTHYRONINE is a medical device that received FDA 510(k) clearance on 1976-09-13. The listed applicant is Smithkline Diagnostics, Inc.. The 510(k) number is K760057.

When did TEST, RIA, TRIODOTHYRONINE receive FDA 510(k) clearance?

TEST, RIA, TRIODOTHYRONINE received FDA 510(k) clearance on 1976-09-13, under 510(k) number K760057.

Who is the listed applicant for TEST, RIA, TRIODOTHYRONINE?

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

What is the FDA product code for TEST, RIA, TRIODOTHYRONINE?

The FDA product code for TEST, RIA, TRIODOTHYRONINE 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.

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