TRIOS SYSTEM— 510(k) K090399

Substantially Equivalent

Viora , Ltd.

FDA 510(k) clearance K090399 for TRIOS SYSTEM, Substantially Equivalent on 2009-06-10. Applicant: Viora , Ltd.. Device class: 2.

Clearance details

Applicant: Viora , Ltd.
Product code: Code ONF
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2009-02-17
Decision date: 2009-06-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Jersey City, NJ, 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.