AliveCor, Inc.

19 FDA 510(k) medical device clearances.

Top product codes for AliveCor, Inc.

Recent clearances by AliveCor, Inc.

K252589 — Corvair Monza MHX · 2026-01-09
K231010 — Corvair MHX · 2024-06-07
K232035 — Impala DPS · 2024-06-07
K220350 — KardiaMobile 6L DXH · 2022-05-25
K212662 — AliveCor QT Service DQK · 2022-04-26
K211668 — KardiaMobile Card DXH · 2021-11-30
K210753 — KardiaMobile 6L DXH · 2021-06-30
K201985 — KardiaAI DQK · 2020-11-12
K191406 — KardiaMobile, KardiaStation DXH · 2020-01-24
K183319 — Triangle System DXH · 2019-05-10
K182396 — KardiaMobile, KardiaStation DXH · 2019-04-12
K181823 — KardiaAI DQK · 2019-03-11
K171816 — Kardia Band System DXH · 2017-11-16
K142743 — AliveCor Heart Monitor DXH · 2015-01-27
K142672 — AliveCor Heart Monitor DXH · 2014-12-03
K140933 — ALIVECOR HEART MONITOR DXH · 2014-08-15
K130921 — ALIVECOR HEART MONITOR OTC DPS · 2014-02-06
K130409 — ALIVECOR HEART MONITOR DPS · 2013-09-06
K122356 — ALIVECOR HEART MONITOR FOR IPHONE DPS · 2012-11-19

Data sourced from openFDA. This site is unofficial and independent of the FDA.