Quantum Perfusion Dual Lumen Cannula 31F, Quantum Perfusion Dual Lumen Cannula 27F, Quantum Perfusion Dual Lumen Cannula 24F, Quantum Perfusion Dual Lumen Cannula 29F, Quantum Perfusion Dual Lumen Cannula 24F-V1, Quantum Perfusion Dual Lumen Cannula 27F-V1, Quantum Perfusion Dual Lumen Cannula 29F-V1, Quantum Perfusion Dual Lumen Cannula 27F-VS, Quantum Perfusion Dual Lumen Cannula 31F-VS

FDA 510(k) K221353 · Qura S.R.L

Substantially Equivalent

510(k) numberK221353

Submission

Device name
Quantum Perfusion Dual Lumen Cannula 31F, Quantum Perfusion Dual Lumen Cannula 27F, Quantum Perfusion Dual Lumen Cannula 24F, Quantum Perfusion Dual Lumen Cannula 29F, Quantum Perfusion Dual Lumen Cannula 24F-V1, Quantum Perfusion Dual Lumen Cannula 27F-V1, Quantum Perfusion Dual Lumen Cannula 29F-V1, Quantum Perfusion Dual Lumen Cannula 27F-VS, Quantum Perfusion Dual Lumen Cannula 31F-VS
Applicant
Qura S.R.L
Mirandola, IT
Received
May 10, 2022
Decision date
August 18, 2022
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DWF – Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4210
Specialty
Cardiovascular

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K260043Smart Reactors Camouflage Coated Extracorporeal Cardiopulmonary Tubing Set (SR180C)DWF · Traditional Smart Reactors02/23/2026SE
K253203Retrograde Coronary Sinus Perfusion CannulaeDWF · Traditional Medtronic, Inc.02/19/2026SE
K253671Dual Stage Venous CannulaeDWF · Traditional Sorin Group Italia S.R.L.01/30/2026SE
K253998Clearview Intracoronary ShuntsDWF · Special Medtronic, Inc.01/20/2026SE
K253106AngioVac CannulaDWF · Special AngioDynamics, Inc.10/24/2025SE
K250283RAP Femoral Venous CannulaeDWF · Special LivaNova USA, Inc.07/10/2025SE
K250610Easyflow (103-200; 103-300); Easyflow Duo (103-210; 103-310)DWF · Special Sorin Group Italia S.R.L.06/27/2025SE
K251258MC2™ Two-Stage Venous Cannula; MC2X™ Three-Stage Venous CannulaDWF · Traditional Medtronic, Inc.06/20/2025SE

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K213540Quantum SuperPAC Tubing Set, Quantum SuperPAC Cardioplegia SetDWF · Traditional 05/20/2022SE
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Questions and answers

When was Quantum Perfusion Dual Lumen Cannula 31F, Quantum Perfusion Dual Lumen Cannula 27F, Quantum Perfusion Dual Lumen Cannula 24F, Quantum Perfusion Dual Lumen Cannula 29F, Quantum Perfusion Dual Lumen Cannula 24F-V1, Quantum Perfusion Dual Lumen Cannula 27F-V1, Quantum Perfusion Dual Lumen Cannula 29F-V1, Quantum Perfusion Dual Lumen Cannula 27F-VS, Quantum Perfusion Dual Lumen Cannula 31F-VS cleared by the FDA?

Quantum Perfusion Dual Lumen Cannula 31F, Quantum Perfusion Dual Lumen Cannula 27F, Quantum Perfusion Dual Lumen Cannula 24F, Quantum Perfusion Dual Lumen Cannula 29F, Quantum Perfusion Dual Lumen Cannula 24F-V1, Quantum Perfusion Dual Lumen Cannula 27F-V1, Quantum Perfusion Dual Lumen Cannula 29F-V1, Quantum Perfusion Dual Lumen Cannula 27F-VS, Quantum Perfusion Dual Lumen Cannula 31F-VS (K221353) received a 510(k) decision of Substantially Equivalent on August 18, 2022, 100 days after the submission was received.

What is the product code of K221353?

The FDA product code is DWF – Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass, a Class II (moderate risk) device regulated under 21 CFR 870.4210.