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

FDA 510(k) Number Submission Date Device Name Applicant
K140933 04/11/2014 ALIVECOR HEART MONITOR ALIVECOR, INC.
K142672 09/19/2014 AliveCor Heart Monitor ALIVECOR, INC.
K142743 09/24/2014 AliveCor Heart Monitor AliveCor, Inc.
K130409 02/19/2013 ALIVECOR HEART MONITOR ALIVECOR, INC.
K130921 04/03/2013 ALIVECOR HEART MONITOR OTC ALIVECOR, INC.
K122356 08/03/2012 ALIVECOR HEART MONITOR FOR IPHONE ALIVECOR, INC.
K181823 07/09/2018 KardiaAI AliveCor, Inc.
K182396 09/04/2018 KardiaMobile, KardiaStation AliveCor, Inc.
K183319 11/30/2018 Triangle System AliveCor, Inc.
K210753 03/15/2021 KardiaMobile 6L AliveCor, Inc.
K191406 05/28/2019 KardiaMobile, KardiaStation AliveCor, Inc.
K211668 06/01/2021 KardiaMobile Card AliveCor, Inc.
K201985 07/17/2020 KardiaAI AliveCor, Inc.
K220350 02/07/2022 KardiaMobile 6L AliveCor, Inc.
K212662 08/23/2021 AliveCor QT Service AliveCor, Inc.


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