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EMISSION TOMOGRAPHY CAROUSEL

K896151 Class II Traditional
Decision Date
1991-04-16
Sponsor / Applicant
Atf Consolidated

Technical Specification

510(k) Submission ID K896151
Product Code KPS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1200
Decision Date 1991-04-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMISSION TOMOGRAPHY CAROUSEL received FDA 510(k) clearance under submission number K896151, sponsored by Atf Consolidated. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1991-04-16.

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.