ViMove2
K-Number: K163150 · 2017-07-14
ApplicantDorsavi, Ltd.
Decision Date2017-07-14
Product CodeIKN
Advisory CommitteePM
DecisionSubstantially Equivalent
Device Summary
ViMove2 is a medical device manufactured by Dorsavi, Ltd.. It received FDA 510(k) clearance on 2017-07-14 under approval number K163150. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ViMove2?
ViMove2 is a medical device that received FDA 510(k) clearance on 2017-07-14. It is manufactured by Dorsavi, Ltd.. The 510(k) number is K163150.
When was ViMove2 approved by the FDA?
ViMove2 received FDA 510(k) clearance on 2017-07-14, under approval number K163150.
What company makes ViMove2?
ViMove2 is manufactured by Dorsavi, Ltd..
What is the FDA product code for ViMove2?
The FDA product code for ViMove2 is IKN.
Related Devices (Code: IKN)
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.