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ACCUSPEC THYROID UPTAKE SYSTEM SOFTWARE

K896540 Class I Traditional
Decision Date
1990-04-19
Sponsor / Applicant
Nuclear Data Systems

Technical Specification

510(k) Submission ID K896540
Product Code IZD
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1320
Decision Date 1990-04-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACCUSPEC THYROID UPTAKE SYSTEM SOFTWARE received FDA 510(k) clearance under submission number K896540, sponsored by Nuclear Data Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1990-04-19.

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.