# K950004: Heartview (TM) 12-Lead Electrocardiograph Recorder/Transmitter

- Pathway: 510(k) (Traditional)
- Applicant: Aerotel, Ltd.
- Decided: Oct 24, 1995 after 294 days
- Product code: DPS (Electrocardiograph)
- Device class: 2
- Regulation: 21 CFR 870.2340
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
16 later devices descend from it; 3 cite it directly.
0 of 17 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
- K983717: BP-Tel Trans-Telephonic Blood Pressure Measurement System (1999), 11 descendants of its own
- K021447: Tele-Cliniq Data Transmission System Blood Pressure Measurement System (2002), 10 descendants of its own
- K030825: MPM-Net (2003), 9 descendants of its own
- K041854: MPM System (2004), 8 descendants of its own
- K051544: Vitalcaregiving System (2005), 7 descendants of its own

Source page: https://510kreport.com/device/K950004
Methodology: https://510kreport.com/methodology