INMODE SR IPL DEVICE— 510(k) K123860

Substantially Equivalent

Inmode MD , Ltd.

FDA 510(k) clearance K123860 for INMODE SR IPL DEVICE, Substantially Equivalent on 2013-04-02. Applicant: Inmode MD , Ltd.. Device class: 2.

Clearance details

Applicant: Inmode MD , Ltd.
Product code: Code ONF
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2012-12-14
Decision date: 2013-04-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kfar Saba, IL

Download summary PDF View on FDA.gov ↗

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