VITESSE 3.0— 510(k) K123152

Name: FDA 510(k) clearance K123152
Creator: U.S. Food and Drug Administration
Published: 2012-12-07

Substantially Equivalent

Varian Medical Systems, Oncology Systems

FDA 510(k) clearance K123152 for VITESSE 3.0, Substantially Equivalent on 2012-12-07. Applicant: Varian Medical Systems, Oncology Systems. Device class: 2.

Clearance details

Applicant: Varian Medical Systems, Oncology Systems
Product code: Code MUJ
Device class: Class 2
Regulation: 21 CFR 892.5050
Advisory panel: Radiology
Date received: 2012-10-09
Decision date: 2012-12-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palo Alto, CA, US

Download summary PDF View on FDA.gov ↗

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