# K864260: Applicard System (Ecg Electrode System)

- Pathway: 510(k) (Traditional)
- Applicant: Grandcor Medical Systems
- Decided: May 11, 1987 after 194 days
- Product code: DRX (Electrode, Electrocardiograph)
- Device class: 2
- Regulation: 21 CFR 870.2360
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 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
- K954772: Quickels QS 200 System (1996), 0 descendants of its own
- K954773: Quickels QS 100 System (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K864260
Methodology: https://510kreport.com/methodology