ProCinch, QuadCinch
K-Number: K240194 · 2024-02-21
ApplicantRiverpoint Medical
Decision Date2024-02-21
Product CodeMBI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
ProCinch, QuadCinch is a medical device manufactured by Riverpoint Medical. It received FDA 510(k) clearance on 2024-02-21 under approval number K240194. The device is classified under product code MBI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ProCinch, QuadCinch?
ProCinch, QuadCinch is a medical device that received FDA 510(k) clearance on 2024-02-21. It is manufactured by Riverpoint Medical. The 510(k) number is K240194.
When was ProCinch, QuadCinch approved by the FDA?
ProCinch, QuadCinch received FDA 510(k) clearance on 2024-02-21, under approval number K240194.
What company makes ProCinch, QuadCinch?
ProCinch, QuadCinch is manufactured by Riverpoint Medical.
What is the FDA product code for ProCinch, QuadCinch?
The FDA product code for ProCinch, QuadCinch is MBI.
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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.