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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