VIVIX-S— 510(k) K120020

Substantially Equivalent

Vieworks Co., Ltd.

FDA 510(k) clearance K120020 for VIVIX-S, Substantially Equivalent on 2012-05-04. Applicant: Vieworks Co., Ltd.. Device class: 2.

Clearance details

Applicant: Vieworks Co., Ltd.
Product code: Code MQB
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 2012-01-03
Decision date: 2012-05-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fullerton, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.