# K890079: Lifepak 10 Defibrillator/Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Physio-Control Corp.
- Decided: Feb 23, 1989 after 50 days
- Product code: LDD (Dc-Defibrillator, Low-Energy, (Including Paddles))
- Device class: 2
- Regulation: 21 CFR 870.5300
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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.

## Recalls of this device
- Feb 27, 2008 · Not classified · Z-1567-2008: Batteries mislabeled - batteries labeled as 2.4 amp/hour batteries, however are 1.0 amp/hour batteries.

Source page: https://510kreport.com/device/K890079
Methodology: https://510kreport.com/methodology