# K022210: Multifunctional Electrode Models 9640, 9650

- Pathway: 510(k) (Traditional)
- Applicant: Cardiac Science, Inc.
- Decided: Oct 4, 2002 after 88 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
Longest line of descent: 1 generation back to K960329 (1996). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K960329: Disposable Hydrogel Defibrillation Electrode/Pad, Contour Medical Technology, Inc. (1996) Summary page 2.

## Indications for use
The Multifunctional Electrodes are single use and intended to be used for defibrillation, synchronized cardioversion, ECG monitoring and external pacing.

Source page: https://510kreport.com/device/K022210
Methodology: https://510kreport.com/methodology