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FDA 510(k)

MC3 QuickFlow Dual Lumen Catheter

K-Number: K171610 · 2017-11-16

ApplicantMc3 Incorporated
Decision Date2017-11-16
Product CodePZS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MC3 QuickFlow Dual Lumen Catheter is a medical device manufactured by Mc3 Incorporated. It received FDA 510(k) clearance on 2017-11-16 under approval number K171610. The device is classified under product code PZS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MC3 QuickFlow Dual Lumen Catheter?

MC3 QuickFlow Dual Lumen Catheter is a medical device that received FDA 510(k) clearance on 2017-11-16. It is manufactured by Mc3 Incorporated. The 510(k) number is K171610.

When was MC3 QuickFlow Dual Lumen Catheter approved by the FDA?

MC3 QuickFlow Dual Lumen Catheter received FDA 510(k) clearance on 2017-11-16, under approval number K171610.

What company makes MC3 QuickFlow Dual Lumen Catheter?

MC3 QuickFlow Dual Lumen Catheter is manufactured by Mc3 Incorporated.

What is the FDA product code for MC3 QuickFlow Dual Lumen Catheter?

The FDA product code for MC3 QuickFlow Dual Lumen Catheter is PZS.

Related Clinical Trials

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Other Devices by Mc3 Incorporated

K182914MC3 Vascular Access Kit 21030 K180151MC3 Jugular Dual Lumen Catheter K191935Nautilus Smart ECMO Module

Related Devices (Code: PZS)

K180151MC3 Jugular Dual Lumen CatheterMc3 Incorporated K203409MC3 Crescent Jugular Dual Lumen CatheterMc3, Inc. K232480ProtekDuo Veno-Venous Cannula SetsCardiacassist, Inc.

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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