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FDA 510(k)

RIA KIT, T4 CLASP

K-Number: K770726 · 1977-04-28

ApplicantSquibb & Sons, Inc.
Decision Date1977-04-28
Product CodeCDX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIA KIT, T4 CLASP is the device name listed in this FDA 510(k) record. The listed applicant is Squibb & Sons, Inc.. It received FDA 510(k) clearance on 1977-04-28 under 510(k) number K770726. The device is classified under product code CDX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIA KIT, T4 CLASP?

RIA KIT, T4 CLASP is a medical device that received FDA 510(k) clearance on 1977-04-28. The listed applicant is Squibb & Sons, Inc.. The 510(k) number is K770726.

When did RIA KIT, T4 CLASP receive FDA 510(k) clearance?

RIA KIT, T4 CLASP received FDA 510(k) clearance on 1977-04-28, under 510(k) number K770726.

Who is the listed applicant for RIA KIT, T4 CLASP?

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

What is the FDA product code for RIA KIT, T4 CLASP?

The FDA product code for RIA KIT, T4 CLASP is CDX.

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.

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Other records listing 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.

K821174TSH-SQUIBB RADIOIMMUNOASSAY KITK801424ESTRIOL RIA KIT FOR USE WITH GAMMAFLOK800750STOMAHESIVE STERILE WAFERK761267ANGIOTENSIN I IMMUTOPE KIT

Related Devices (Code: CDX)

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.

K961490ELECSYS T4 ASSAYBoehringer Mannheim Corp.K954312ACTIVE THYROXINE RIADiagnostic Systems Laboratories, Inc.K943416DELFIA NEONATAL THYROXINE KITWallac OYK934384AXSYM(TM) TOTAL T4Abbott LaboratoriesK932980TOTAL T4 FPIA REAGENT SET/CALIBRATOR #T-1039,T-116Sigma Diagnostics, Inc.K933426STRATUS(R) TOTAL THYROXINE(T4) FLUOR ENZYME IMMUNOBaxter Diagnostics, Inc.

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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