Pure-Vu EVS System
K-Number: K232922 · 2023-10-20
ApplicantMotus GI Medical Technologies , Ltd.
Decision Date2023-10-20
Product CodeFDF
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Pure-Vu EVS System is a medical device manufactured by Motus GI Medical Technologies , Ltd.. It received FDA 510(k) clearance on 2023-10-20 under approval number K232922. The device is classified under product code FDF. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Pure-Vu EVS System?
Pure-Vu EVS System is a medical device that received FDA 510(k) clearance on 2023-10-20. It is manufactured by Motus GI Medical Technologies , Ltd.. The 510(k) number is K232922.
When was Pure-Vu EVS System approved by the FDA?
Pure-Vu EVS System received FDA 510(k) clearance on 2023-10-20, under approval number K232922.
What company makes Pure-Vu EVS System?
Pure-Vu EVS System is manufactured by Motus GI Medical Technologies , Ltd..
What is the FDA product code for Pure-Vu EVS System?
The FDA product code for Pure-Vu EVS System is FDF.
Other Devices by Motus GI Medical Technologies , Ltd.
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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.