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FDA 510(k) Applications Submitted by Abbott (formerly Thoratec Corporation)
FDA 510(k) Number
Submission Date
Device Name
Applicant
K200306
02/06/2020
CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula Kit
Abbott (formerly Thoratec Corporation)
K222038
07/11/2022
CentriMagÖ Blood Pump for use with CentriMagÖ Acute Circulatory Support System
Abbott (formerly Thoratec Corporation)
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