# K892005: Shock Advisory Adapter for Use W/Lifepak 9

- Pathway: 510(k) (Traditional)
- Applicant: Physio-Control Corp.
- Decided: Jun 20, 1989 after 84 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. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K954957: Codemaster XL + XL W/Shock Advisory Option (1996), 0 descendants of its own

Source page: https://510kreport.com/device/K892005
Methodology: https://510kreport.com/methodology