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FDA 510(k)

InMode RF System

K-Number: K240780 · 2024-07-24

ApplicantInMode , Ltd.
Decision Date2024-07-24
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

InMode RF System is the device name listed in this FDA 510(k) record. The listed applicant is InMode , Ltd.. It received FDA 510(k) clearance on 2024-07-24 under 510(k) number K240780. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the InMode RF System?

InMode RF System is a medical device that received FDA 510(k) clearance on 2024-07-24. The listed applicant is InMode , Ltd.. The 510(k) number is K240780.

When did InMode RF System receive FDA 510(k) clearance?

InMode RF System received FDA 510(k) clearance on 2024-07-24, under 510(k) number K240780.

Who is the listed applicant for InMode RF System?

The FDA 510(k) record lists InMode , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for InMode RF System?

The FDA product code for InMode RF System is GEI.

Other records listing InMode , Ltd. as applicant

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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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