LEVO COMBI— 510(k) K030893

Substantially Equivalent

Levo AG

FDA 510(k) clearance K030893 for LEVO COMBI, Substantially Equivalent on 2003-04-02. 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: 2003-03-21
Decision date: 2003-04-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: 5610 Wohlen, CH

Download summary PDF View on FDA.gov ↗

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