LEVO C3— 510(k) K083017

Substantially Equivalent

Levo AG

FDA 510(k) clearance K083017 for LEVO C3, Substantially Equivalent on 2008-10-24. Applicant: Levo AG. Device class: 2.

Clearance details

Applicant: Levo AG
Product code: Code IPL
Device class: Class 2
Regulation: 21 CFR 890.3900
Advisory panel: Physical Medicine
Date received: 2008-10-09
Decision date: 2008-10-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: 5610 Wohlen, CH

Download summary PDF View on FDA.gov ↗

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