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CLINICAL ASSAYS(TM) GAMMACOAT(TM) M [125I] T4

K901475 Class II Traditional
Decision Date
1990-06-20
Sponsor / Applicant
Baxter Healthcare Corp

Technical Specification

510(k) Submission ID K901475
Product Code CDX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1700
Decision Date 1990-06-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLINICAL ASSAYS(TM) GAMMACOAT(TM) M [125I] T4 received FDA 510(k) clearance under submission number K901475, sponsored by Baxter Healthcare Corp. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1990-06-20.

Classification & Regulation

This clearance is catalogued under FDA product code CDX and 21 CFR 862.1700, within the Clinical Chemistry review panel as a Class II device.