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FDA 510(k)

InMode System with vTone Applicator

K-Number: K200293 · 2020-05-05

ApplicantInMode , Ltd.
Decision Date2020-05-05
Product CodeKPI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

InMode System with vTone Applicator is a medical device manufactured by InMode , Ltd.. It received FDA 510(k) clearance on 2020-05-05 under approval number K200293. The device is classified under product code KPI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the InMode System with vTone Applicator?

InMode System with vTone Applicator is a medical device that received FDA 510(k) clearance on 2020-05-05. It is manufactured by InMode , Ltd.. The 510(k) number is K200293.

When was InMode System with vTone Applicator approved by the FDA?

InMode System with vTone Applicator received FDA 510(k) clearance on 2020-05-05, under approval number K200293.

What company makes InMode System with vTone Applicator?

InMode System with vTone Applicator is manufactured by InMode , Ltd..

What is the FDA product code for InMode System with vTone Applicator?

The FDA product code for InMode System with vTone Applicator is KPI.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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