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FDA 510(k)

T3 CLASP RIA KIT

K-Number: K771142 · 1977-07-14

Decision Date1977-07-14
Product CodeCDP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

T3 CLASP 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 1977-07-14 under 510(k) number K771142. 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 CLASP RIA KIT?

T3 CLASP RIA KIT is a medical device that received FDA 510(k) clearance on 1977-07-14. The listed applicant is E. R. Squibb & Sons, Inc.. The 510(k) number is K771142.

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

T3 CLASP RIA KIT received FDA 510(k) clearance on 1977-07-14, under 510(k) number K771142.

Who is the listed applicant for T3 CLASP 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 CLASP RIA KIT?

The FDA product code for T3 CLASP RIA KIT is CDP.

Related Clinical Trials

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.

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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