FDA 510(k)

CBR-T3RIA KIT

K-Number: K780499 · 1978-05-04

Decision Date1978-05-04

Product CodeCDP

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

CBR-T3RIA KIT is the device name listed in this FDA 510(k) record. The listed applicant is Clinical Bioresearch. It received FDA 510(k) clearance on 1978-05-04 under 510(k) number K780499. 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 CBR-T3RIA KIT?

CBR-T3RIA KIT is a medical device that received FDA 510(k) clearance on 1978-05-04. The listed applicant is Clinical Bioresearch. The 510(k) number is K780499.

When did CBR-T3RIA KIT receive FDA 510(k) clearance?

CBR-T3RIA KIT received FDA 510(k) clearance on 1978-05-04, under 510(k) number K780499.

Who is the listed applicant for CBR-T3RIA KIT?

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

What is the FDA product code for CBR-T3RIA KIT?

The FDA product code for CBR-T3RIA KIT is CDP.

Other records listing Clinical Bioresearch 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.

K780707T4-RIA KIT K780500CBR-T3 UPTAKE KIT K780498CBR-DIGOXIN ANTISERUM

Related Devices (Code: CDP)

K001607REPROBEAD T3 ENZYME IMMUNOASSAY REAGENT KIT (CATALOG# 104)Repromedix Corp.K991692CHIRON DIAGNOSTICS ACS: 180 FT3Chiron Diagnostics Corp.K991311TOTAL T3 ENZYME IMMUNOASSAY TEST KIT, MODEL BC-1005Biocheck, Inc.K991252AIA-PACK FT3 ASSAYTosoh Medics, Inc.K981824OPTICOAT T3 EIA KITBiotecx Laboratories, Inc.K983439ABBOTT ARCHITECT FREE T3Abbott Laboratories

Official Source

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