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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Riverpoint Medical. It received FDA 510(k) clearance on 2024-02-21 under 510(k) 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. The listed applicant is Riverpoint Medical. The 510(k) number is K240194.

When did ProCinch, QuadCinch receive FDA 510(k) clearance?

ProCinch, QuadCinch received FDA 510(k) clearance on 2024-02-21, under 510(k) number K240194.

Who is the listed applicant for ProCinch, QuadCinch?

The FDA 510(k) record lists Riverpoint Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ProCinch, QuadCinch?

The FDA product code for ProCinch, QuadCinch is MBI.

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Related Devices (Code: 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.

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