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THYROID UPTAKE SYSTEM

K833140 Class I Traditional
Decision Date
1983-12-08
Sponsor / Applicant
Advanced Medical Research Corp.

Technical Specification

510(k) Submission ID K833140
Product Code IZD
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1320
Decision Date 1983-12-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THYROID UPTAKE SYSTEM received FDA 510(k) clearance under submission number K833140, sponsored by Advanced Medical Research Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1983-12-08.

Classification & Regulation

This clearance is catalogued under FDA product code IZD and 21 CFR 892.1320, within the Radiology review panel as a Class I device.