InMode PLUS System
K-Number: K172302 · 2017-12-08
ApplicantInmode MD , Ltd.
Decision Date2017-12-08
Product CodePBX
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
InMode PLUS System is a medical device manufactured by Inmode MD , Ltd.. It received FDA 510(k) clearance on 2017-12-08 under approval number K172302. The device is classified under product code PBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the InMode PLUS System?
InMode PLUS System is a medical device that received FDA 510(k) clearance on 2017-12-08. It is manufactured by Inmode MD , Ltd.. The 510(k) number is K172302.
When was InMode PLUS System approved by the FDA?
InMode PLUS System received FDA 510(k) clearance on 2017-12-08, under approval number K172302.
What company makes InMode PLUS System?
InMode PLUS System is manufactured by Inmode MD , Ltd..
What is the FDA product code for InMode PLUS System?
The FDA product code for InMode PLUS System is PBX.
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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.