# K952065: Paceart Cardiovoice

- Pathway: 510(k) (Traditional)
- Applicant: Paceart, Inc.
- Decided: Jan 16, 1996 after 259 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.
5 later devices descend from it; 3 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K024278: Paceart System (2003), 2 descendants of its own
- K110693: Paceart Optima System Software (2011), 1 descendant of its own
- K142349: TM eCloud ECG Analysis System (2015), 0 descendants of its own
- K991211: Eventstation Ecg Trans-Telephonic Receiving System (1999), 0 descendants of its own
- K982034: E-Fax System (1999), 0 descendants of its own

Source page: https://510kreport.com/device/K952065
Methodology: https://510kreport.com/methodology