LEVO MOBIL LCM— 510(k) K963817

Substantially Equivalent

Levo USA

FDA 510(k) clearance K963817 for LEVO MOBIL LCM, Substantially Equivalent on 1997-12-23. Applicant: Levo USA. Device class: 2.

Clearance details

Applicant: Levo USA
Product code: Code IPL
Device class: Class 2
Regulation: 21 CFR 890.3900
Advisory panel: Physical Medicine
Date received: 1996-09-23
Decision date: 1997-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dottikon, CH

Download summary PDF View on FDA.gov ↗

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More clearances from Levo USA

K973951 — LEVO COMPACT-EASY LCE1997-12-23
K971873 — LEVO ACTIVE-EASY LAE1997-07-03
K963816 — LEVO COMPACT LC1996-10-30

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