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CIRRUS GAMMA CAMERA

K913471 Class II Traditional
Decision Date
1991-10-23
Sponsor / Applicant
Adac Laboratories

Technical Specification

510(k) Submission ID K913471
Product Code KPS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1200
Decision Date 1991-10-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CIRRUS GAMMA CAMERA received FDA 510(k) clearance under submission number K913471, sponsored by Adac Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1991-10-23.

Classification & Regulation

This clearance is catalogued under FDA product code KPS and 21 CFR 892.1200, within the Radiology review panel as a Class II device.