FDA 510(k) Applications Submitted by CardiacAssist, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K232132 07/18/2023 LifeSPARC System CardiacAssist, Inc.
K232480 08/16/2023 ProtekDuo Veno-Venous Cannula Sets CardiacAssist, Inc.
K211830 06/14/2021 LifeSPARC System CardiacAssist, Inc.
K202751 09/21/2020 TandemHeart Pump and Escort Controller CardiacAssist, Inc.


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