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 a medical device manufactured by InMode , Ltd.. It received FDA 510(k) clearance on 2024-07-24 under approval 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. It is manufactured by InMode , Ltd.. The 510(k) number is K240780.
When was InMode RF System approved by the FDA?
InMode RF System received FDA 510(k) clearance on 2024-07-24, under approval number K240780.
What company makes InMode RF System?
InMode RF System is manufactured by InMode , Ltd..
What is the FDA product code for InMode RF System?
The FDA product code for InMode RF System is GEI.
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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.