InMode Plus System
K-Number: K153568 · 2016-07-12
ApplicantInmode MD , Ltd.
Decision Date2016-07-12
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 2016-07-12 under approval number K153568. 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 2016-07-12. It is manufactured by Inmode MD , Ltd.. The 510(k) number is K153568.
When was InMode Plus System approved by the FDA?
InMode Plus System received FDA 510(k) clearance on 2016-07-12, under approval number K153568.
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.