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

K241352 Class II Special
Decision Date
2024-06-12
Sponsor / Applicant
Medtronic, Inc.

Technical Specification

510(k) Submission ID K241352
Product Code DTZ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4350
Decision Date 2024-06-12
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Affinity NT Oxygenator and Uncoated Cardiotomy/ Venous Reservoir (541); Affinity NT Oxygenator with Balance Biosurface and Uncoated Cardiotomy/Venous Reservoir (541B) received FDA 510(k) clearance under submission number K241352, sponsored by Medtronic, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2024-06-12.

Classification & Regulation

This clearance is catalogued under FDA product code DTZ and 21 CFR 870.4350, within the Cardiovascular review panel as a Class II device.