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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