# K982896: Alexander Manufacturing CO. Rechargeable Battery Part Number LP9

- Pathway: 510(k) (Traditional)
- Applicant: Alexander Mfg. Co.
- Decided: Oct 21, 1998 after 65 days
- Product code: LDD (Dc-Defibrillator, Low-Energy, (Including Paddles))
- Device class: 2
- Regulation: 21 CFR 870.5300
- 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 K935674 (1993). 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)
- K935674: Lifepak 9 Defibrillator/Monitor, Physio-Control Corp. (1993) Summary page 3.

## Indications for use
Replacement battery for Physio-Control 803704-01 Life-Pak 9 Low-Energy Cardiac Monitor/Defibrillator, 510(k) Number 935674. This battery is shipped only to customers who request a replacement battery for a particular device or to replace a competitor’s replacement battery. The biomedical equipment technician therefore knows the intended use is as a replacement battery.

Source page: https://510kreport.com/device/K982896
Methodology: https://510kreport.com/methodology