# K002806: K-Defib/Pace, Model KDP-60A

- Pathway: 510(k) (Traditional)
- Applicant: Katecho, Inc.
- Decided: Nov 21, 2000 after 74 days
- Product code: MKJ (Automated External Defibrillators (Non-Wearable))
- Device class: 3
- Regulation: 21 CFR 870.5310
- 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.
1 of 5 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K014209: Padpro  Model 2001, 2001-S, 2001-C, 2001-Eps (2002), 2 descendants of its own
- K103186: Skintact Radiotransparent Multifunction Electrodes (2011), 0 descendants of its own
- K042088: Samaritan Pad Pak Defibrillation Electrode, Model SPP-301 (2004), 0 descendants of its own
- K020743: Padpro, Model 2502 (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K002806
Methodology: https://510kreport.com/methodology