InMode PLUS System— 510(k) K172302

Substantially Equivalent

Inmode MD , Ltd.

FDA 510(k) clearance K172302 for InMode PLUS System, Substantially Equivalent on 2017-12-08. Applicant: Inmode MD , Ltd.. Device class: 2.

Clearance details

Applicant: Inmode MD , Ltd.
Product code: Code PBX
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 2017-07-31
Decision date: 2017-12-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Yokneam, IL

Download summary PDF View on FDA.gov ↗

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More clearances from Inmode MD , Ltd.

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K183450 — EmBody System2019-06-20
K182325 — InMode RF System2018-09-26

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