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PORTALVISION ADVANCED IMAGING

K091209 Class II Traditional
Decision Date
2009-06-23
Sponsor / Applicant
Varian Medical Systems, Inc.

Technical Specification

510(k) Submission ID K091209
Product Code IYE
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 2009-06-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PORTALVISION ADVANCED IMAGING received FDA 510(k) clearance under submission number K091209, sponsored by Varian Medical Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2009-06-23.

Classification & Regulation

This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.