meddevicedb.com FDA Device Reference

TIPSEP-T4(RIA) T4 RADIOIMMUNOASSAY

K792599 Class II Traditional
Decision Date
1980-01-16
Sponsor / Applicant
Nuclear Diagnostics, Inc.

Technical Specification

510(k) Submission ID K792599
Product Code CDX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1700
Decision Date 1980-01-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TIPSEP-T4(RIA) T4 RADIOIMMUNOASSAY received FDA 510(k) clearance under submission number K792599, 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 1980-01-16.

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.