# K870880: EK10 Electrocardiograph

- Pathway: 510(k) (Traditional)
- Applicant: Burdick Corp.
- Decided: Apr 9, 1987 after 36 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.
3 later devices descend from it; 2 cite it directly.
0 of 4 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
- K103706: The Core (Cardiac Outpatient Realtime Ecg) Monitor (2011), 1 descendant of its own
- K160667: Anybattery C2 Rechargeable Battery (2017), 0 descendants of its own
- K142352: CardiacLinx (2015), 0 descendants of its own

Source page: https://510kreport.com/device/K870880
Methodology: https://510kreport.com/methodology