# K914955: K-Defib/Pace Electrode

- Pathway: 510(k) (Traditional)
- Applicant: Katecho, Inc.
- Decided: May 14, 1992 after 191 days
- Product code: DRO (Pacemaker, Cardiac, External Transcutaneous (Non-Invasive))
- Device class: 2
- Regulation: 21 CFR 870.5550
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 1 cites it directly.
1 of 8 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
- K971149: SVL-9130 Defibrillation Electrode (1997), 6 descendants of its own
- K082090: 9131 Defibrillation Electrodes (2008), 4 descendants of its own
- K122758: Powerheart G5 Aed (2014), 1 descendant of its own
- K143714: Powerheart G5 AED (2015), 0 descendants of its own
- K142803: Skintact, various other tradenames (2014), 0 descendants of its own

Source page: https://510kreport.com/device/K914955
Methodology: https://510kreport.com/methodology