InMode RF Pro System
K-Number: K210492 · 2021-07-12
ApplicantInmode MD , Ltd.
Decision Date2021-07-12
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
InMode RF Pro System is a medical device manufactured by Inmode MD , Ltd.. It received FDA 510(k) clearance on 2021-07-12 under approval number K210492. 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 Pro System?
InMode RF Pro System is a medical device that received FDA 510(k) clearance on 2021-07-12. It is manufactured by Inmode MD , Ltd.. The 510(k) number is K210492.
When was InMode RF Pro System approved by the FDA?
InMode RF Pro System received FDA 510(k) clearance on 2021-07-12, under approval number K210492.
What company makes InMode RF Pro System?
InMode RF Pro System is manufactured by Inmode MD , Ltd..
What is the FDA product code for InMode RF Pro System?
The FDA product code for InMode RF Pro 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.