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REAGENT, RIA TRIIODOTHYRONINE T3 (#200)

K760078 Class II Traditional
Decision Date
1976-07-20
Sponsor / Applicant
Oxford Laboratories, Inc.

Technical Specification

510(k) Submission ID K760078
Product Code CDP
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1710
Decision Date 1976-07-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

REAGENT, RIA TRIIODOTHYRONINE T3 (#200) received FDA 510(k) clearance under submission number K760078, sponsored by Oxford Laboratories, Inc.. 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 1976-07-20.

Classification & Regulation

This clearance is catalogued under FDA product code CDP and 21 CFR 862.1710, within the Clinical Chemistry review panel as a Class II device.