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UNIVERSAL SYSTEM, MODEL QV-800

K023008 Class II Traditional
Decision Date
2002-11-13
Sponsor / Applicant
Quantum Medical Imaging, LLC

Technical Specification

510(k) Submission ID K023008
Product Code KPR
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1680
Decision Date 2002-11-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

UNIVERSAL SYSTEM, MODEL QV-800 received FDA 510(k) clearance under submission number K023008, sponsored by Quantum Medical Imaging, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2002-11-13.

Classification & Regulation

This clearance is catalogued under FDA product code KPR and 21 CFR 892.1680, within the Radiology review panel as a Class II device.