Ventripoint Medical System Plus (VMS+)
K-Number: K173810 · 2018-05-14
ApplicantVentripoint Diagnostics , Ltd.
Decision Date2018-05-14
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Ventripoint Medical System Plus (VMS+) is a medical device manufactured by Ventripoint Diagnostics , Ltd.. It received FDA 510(k) clearance on 2018-05-14 under approval number K173810. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Ventripoint Medical System Plus (VMS+)?
Ventripoint Medical System Plus (VMS+) is a medical device that received FDA 510(k) clearance on 2018-05-14. It is manufactured by Ventripoint Diagnostics , Ltd.. The 510(k) number is K173810.
When was Ventripoint Medical System Plus (VMS+) approved by the FDA?
Ventripoint Medical System Plus (VMS+) received FDA 510(k) clearance on 2018-05-14, under approval number K173810.
What company makes Ventripoint Medical System Plus (VMS+)?
Ventripoint Medical System Plus (VMS+) is manufactured by Ventripoint Diagnostics , Ltd..
What is the FDA product code for Ventripoint Medical System Plus (VMS+)?
The FDA product code for Ventripoint Medical System Plus (VMS+) is IYN.
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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.