meddevicedb.com FDA Device Reference

SUMMIT NUCLEAR VISION FX 20 SERIES GAMMA CAMERA SYSTEMS

K935318 Class II Traditional
Decision Date
1994-02-25
Sponsor / Applicant
Summit Nuclear

Technical Specification

510(k) Submission ID K935318
Product Code KPS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1200
Decision Date 1994-02-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SUMMIT NUCLEAR VISION FX 20 SERIES GAMMA CAMERA SYSTEMS received FDA 510(k) clearance under submission number K935318, sponsored by Summit Nuclear. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1994-02-25.

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.