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FDA 510(k)

T3 RIA KIT

K-Number: K810211 · 1981-02-10

Decision Date1981-02-10
Product CodeCDP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

T3 RIA KIT is the device name listed in this FDA 510(k) record. The listed applicant is E. R. Squibb & Sons, Inc.. It received FDA 510(k) clearance on 1981-02-10 under 510(k) number K810211. 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 T3 RIA KIT?

T3 RIA KIT is a medical device that received FDA 510(k) clearance on 1981-02-10. The listed applicant is E. R. Squibb & Sons, Inc.. The 510(k) number is K810211.

When did T3 RIA KIT receive FDA 510(k) clearance?

T3 RIA KIT received FDA 510(k) clearance on 1981-02-10, under 510(k) number K810211.

Who is the listed applicant for T3 RIA KIT?

The FDA 510(k) record lists E. R. Squibb & Sons, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for T3 RIA KIT?

The FDA product code for T3 RIA KIT is CDP.

Other records listing E. R. Squibb & Sons, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 32 devices →

Related Devices (Code: CDP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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