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TIPSEP-T3U TRIIODOTHYRONINE UPTAKE

K792484 Class II Traditional
Decision Date
1979-12-27
Sponsor / Applicant
Nuclear Diagnostics, Inc.

Technical Specification

510(k) Submission ID K792484
Product Code KHQ
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1715
Decision Date 1979-12-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TIPSEP-T3U TRIIODOTHYRONINE UPTAKE received FDA 510(k) clearance under submission number K792484, sponsored by Nuclear Diagnostics, 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 1979-12-27.

Classification & Regulation

This clearance is catalogued under FDA product code KHQ and 21 CFR 862.1715, within the Clinical Chemistry review panel as a Class II device.