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QV-9000 UNIVERSAL SYSTEM

K083181 Class II Special
Decision Date
2008-11-26
Sponsor / Applicant
Quantum Medical Imaging, LLC

Technical Specification

510(k) Submission ID K083181
Product Code KPR
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1680
Decision Date 2008-11-26
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QV-9000 UNIVERSAL SYSTEM received FDA 510(k) clearance under submission number K083181, sponsored by Quantum Medical Imaging, LLC. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2008-11-26.

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.