# K182396: KardiaMobile, KardiaStation

- Pathway: 510(k) (Traditional)
- Applicant: AliveCor, Inc.
- Decided: Apr 12, 2019 after 220 days
- Product code: DXH (Transmitters And Receivers, Electrocardiograph, Telephone)
- Device class: 2
- Regulation: 21 CFR 870.2920
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K191406: KardiaMobile, KardiaStation (2020), 2 descendants of its own
- K240794: Frontier X Plus (2024), 0 descendants of its own
- K211668: KardiaMobile Card (2021), 0 descendants of its own
- K202228: Omron Model BP7900 Blood Pressure Monitor + EKG (2021), 0 descendants of its own

Source page: https://510kreport.com/device/K182396
Methodology: https://510kreport.com/methodology