# K902288: Modified Lifepak 9 Monitor/Defibrillator

- Pathway: 510(k) (Traditional)
- Applicant: Physio-Control Corp.
- Decided: Feb 25, 1991 after 279 days
- Product code: LDD (Dc-Defibrillator, Low-Energy, (Including Paddles))
- Device class: 2
- Regulation: 21 CFR 870.5300
- Recalls of this device: 2 (0 Class I)
- 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
- K160667: Anybattery C2 Rechargeable Battery (2017), 0 descendants of its own

## Recalls of this device
- Nov 17, 2008 · Not classified · Z-2311-2010: Sterilization efficacy could not be confirmed for sterilization methods on External Sterilizable Paddles and Pediatric Paddle attachments.
- Nov 17, 2008 · Not classified · Z-2312-2010: Sterilization efficacy could not be confirmed for sterilization methods on External Sterilizable Paddles and Pediatric Paddle attachments.

Source page: https://510kreport.com/device/K902288
Methodology: https://510kreport.com/methodology