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FDA 510(k)

CENTRIA T3 RIA

K-Number: K761305 · 1976-12-30

ApplicantUnion Carbide Corp.
Decision Date1976-12-30
Product CodeCDP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

CENTRIA T3 RIA is the device name listed in this FDA 510(k) record. The listed applicant is Union Carbide Corp.. It received FDA 510(k) clearance on 1976-12-30 under 510(k) number K761305. 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 CENTRIA T3 RIA?

CENTRIA T3 RIA is a medical device that received FDA 510(k) clearance on 1976-12-30. The listed applicant is Union Carbide Corp.. The 510(k) number is K761305.

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

CENTRIA T3 RIA received FDA 510(k) clearance on 1976-12-30, under 510(k) number K761305.

Who is the listed applicant for CENTRIA T3 RIA?

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

What is the FDA product code for CENTRIA T3 RIA?

The FDA product code for CENTRIA T3 RIA is CDP.

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Other records listing Union Carbide Corp. as applicant

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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.

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

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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