# K984286: Heartstream Electrode Adapter

- Pathway: 510(k) (Special)
- Applicant: Hewlett-Packard Co.
- Decided: Dec 17, 1998 after 16 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Heartstream Electrode Adapter: named in the summary without a submission number

## Most influential descendants
- K040056: Bio-Detek Electrode Adapter, Model R2001-90 (2004), 0 descendants of its own

## Indications for use
Heartstream Electrode Adapter. For use with Automatic and Manual External Defibrillators and Heartstream Electrodes. For Defibrillation, Monitoring and Pacing.

Source page: https://510kreport.com/device/K984286
Methodology: https://510kreport.com/methodology