meddevicedb.com FDA Device Reference

VISION (NUCLEAR MEDICINE COMPUTER)

K912573 Class II Traditional
Decision Date
1991-10-28
Sponsor / Applicant
Summit Nuclear

Technical Specification

510(k) Submission ID K912573
Product Code KPS
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1200
Decision Date 1991-10-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VISION (NUCLEAR MEDICINE COMPUTER) received FDA 510(k) clearance under submission number K912573, 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 1991-10-28.

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.