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FDA 510(k)

autoLog IQ Autotransfusion System

K-Number: K181954 · 2018-08-22

ApplicantMedtronic Perfusion Systems
Decision Date2018-08-22
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

autoLog IQ Autotransfusion System is a medical device manufactured by Medtronic Perfusion Systems. It received FDA 510(k) clearance on 2018-08-22 under approval number K181954. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the autoLog IQ Autotransfusion System?

autoLog IQ Autotransfusion System is a medical device that received FDA 510(k) clearance on 2018-08-22. It is manufactured by Medtronic Perfusion Systems. The 510(k) number is K181954.

When was autoLog IQ Autotransfusion System approved by the FDA?

autoLog IQ Autotransfusion System received FDA 510(k) clearance on 2018-08-22, under approval number K181954.

What company makes autoLog IQ Autotransfusion System?

autoLog IQ Autotransfusion System is manufactured by Medtronic Perfusion Systems.

What is the FDA product code for autoLog IQ Autotransfusion System?

The FDA product code for autoLog IQ Autotransfusion System is CAC.

Other Devices by Medtronic Perfusion Systems

K240666Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface (BB811); Affinity Fusion Oxygenator with Integrated Arterial Filter and Cardiotomy/Venous Reservoir with Balance Biosurface (BB841); Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface NON STERILE (BB811-NS)

Related Devices (Code: CAC)

K160735CATSmartFresenius Kabi AG K160197Haemonetics Cell Saver Elite Autotransfusion SystemHaemonetics Corporation K162423Haemonetics Cell Saver Elite/Elite+ Autotransfusion SystemHaemonetics Corporation K180831CATSmartFresenius Kabi AG K192368CATSmartFresenius Kabi AG K193361ProCell Surgical Sponge-Blood Recovery UnitProcell Surgical, 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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