Affinity NT Oxygenator and Uncoated Cardiotomy/ Venous Reservoir (541); Affinity NT Oxygenator with Balance Biosurface and Uncoated Cardiotomy/Venous Reservoir (541B)

FDA 510(k) K241352 · Medtronic, Inc.

Substantially Equivalent

510(k) numberK241352

Submission

Device name
Affinity NT Oxygenator and Uncoated Cardiotomy/ Venous Reservoir (541); Affinity NT Oxygenator with Balance Biosurface and Uncoated Cardiotomy/Venous Reservoir (541B)
Applicant
Medtronic, Inc.
Mounds View, MN, US
Received
May 13, 2024
Decision date
June 12, 2024
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DTZ – Oxygenator, Cardiopulmonary Bypass
Device class
Class II (moderate risk)
Regulation
21 CFR 870.4350
Specialty
Cardiovascular
Life-sustaining
Yes

Other 510(k)s with product code DTZ

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K253838Lifemotion Disposable Membrane OxygenatorDTZ · Traditional Lifemotion Medical Technology Co., Ltd.03/16/2026SE
K240934Quantum Perfusion Blood Oxygenator ECC VT160-E3 (VT160-E3); Quantum Perfusion Blood…DTZ · Traditional Spectrum Medical S.R.L.03/12/2026SE
K250821Horizon AF Plus System (Integrated A.L. One AF Plus OXYGENATOR and Horizon CVR)…DTZ · Traditional Eurosets S.R.L12/12/2025SE
K242503Trilly Pediatric Oxygenator with Integrated Arterial Filter (US5232)DTZ · Traditional Eurosets S.R.L11/24/2025SE
K231982Quantum Perfusion Blood Oxygenator VT75-E1, Quantum Perfusion Blood Oxygenator VT75-E2DTZ · Traditional Qura S.R.L09/12/2024SE
K240666Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface…DTZ · Traditional Medtronic Perfusion Systems07/10/2024SE
K231652D100 Kids; D101 KidsDTZ · Special Sorin Group Italia S.R.L.11/16/2023SE
K231773Quantum Perfusion Blood Oxygenator with Integrated AF and Sensor VT75-C1U, Quantum…DTZ · Traditional Qura S.R.L11/08/2023SE
K231414CMO8 Adult PMP Oxygenator with Tubing Pack (Model: CME40009)DTZ · Traditional Chalice Medical , Ltd.11/01/2023SE
K230640Affinity Fusion™ Oxygenator SystemDTZ · Special Medtronic, Inc.04/06/2023SE

More from Medtronic, Inc.

510(k)DeviceDecision
K262735LINQ II Insertable Cardiac Monitor (ICM) (LNQ22)MXD · Special 08/28/2026SE
K262005Affera Integrated Mapping SystemDQK · Special 08/21/2026SE
K261335VitalFlow Set with Balance™ BiosurfaceQJZ · Traditional 07/31/2026SE
K261866Concerto Versa™ Detachable CoilKRD · Special 06/24/2026SE
K253530Trexon™ Monofilament Synthetic Absorbable SutureGAM · Traditional 05/28/2026SE
K260195Elongated One-Piece Arterial (EOPA) 3D™ Arterial CannulaeDWF · Special 04/23/2026SE
K253203Retrograde Coronary Sinus Perfusion CannulaeDWF · Traditional 02/19/2026SE
K253998Clearview Intracoronary ShuntsDWF · Special 01/20/2026SE
K251744Affinity Pixie™ Arterial Filter with Balance™ Biosurface; Affinity® Pediatric Arterial…DTM · Special 01/16/2026SE
K251831Bio-Medicus Life Support Catheter and IntroducerQHW · Traditional 01/15/2026SE

Questions and answers

When was Affinity NT Oxygenator and Uncoated Cardiotomy/ Venous Reservoir (541); Affinity NT Oxygenator with Balance Biosurface and Uncoated Cardiotomy/Venous Reservoir (541B) cleared by the FDA?

Affinity NT Oxygenator and Uncoated Cardiotomy/ Venous Reservoir (541); Affinity NT Oxygenator with Balance Biosurface and Uncoated Cardiotomy/Venous Reservoir (541B) (K241352) received a 510(k) decision of Substantially Equivalent on June 12, 2024, 30 days after the submission was received.

What is the product code of K241352?

The FDA product code is DTZ – Oxygenator, Cardiopulmonary Bypass, a Class II (moderate risk) device regulated under 21 CFR 870.4350.