# K032051: Battery Pack, Rechargeable, Models MLA0051, MLA90479, MNC5169L/P, MNC1000EKG, MNC14649P

- Pathway: 510(k) (Traditional)
- Applicant: Access Battery, Inc.
- Decided: Jan 9, 2004 after 191 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
Longest line of descent: 4 generations back to K844187 (1985). 18 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982135: Oscillomate Ems Nibp Monitor Model 9001, Cas Medical Systems, Inc. (1998) Summary page 2.
- K925402: Oscillomate Blood Pressure Monitor-Model 9300, Cas Medical Systems, Inc. (1993) Summary page 2.
- K925510: Model 90478 & 90479 Telemetry Rec. Module&Housing, Spacelabs Medical, Inc. (1994) Summary page 2.
- K882067: Marquette 1200 Defibrillator, Marquette Electronics, Inc. (1988) Summary page 2.
- K890875: Cardiotest EK53/EK53R, Cardiognost EK56/EK512, Ppg Industries, Inc. (1989) Summary page 2.
- K832015: Multiscriptor EK Various  #43, Litton Medical Electronics (1983) Summary page 2.
- K802718: Model 4700A Electrocardiograph, Hewlett-Packard Co. (1980) Summary page 2.
- K952085: DPD Defibrillator, Medical Research Laboratories, Inc. (1995) Summary page 2.
- K930548: DPD Defibrillator, Medical Research Laboratories, Inc. (1993) Summary page 2.
- K946281: Eclipse 4 Electrocardiograph, Burdick, Inc. (1996)
- K943959: Eclipse 4 Electrocardiograph, Burdick, Inc. (1995) Summary page 2.
- K970920: Siemens SC9000/SC9015 Bedside Monitoring System, Siemens Medical Solutions USA, Inc. (1997) Summary page 2.
- K962291: Siemens SC9000/SC9015 Bedside Monitoring System, Siemens Medical Solutions USA, Inc. (1997) Summary page 2.

## Most influential descendants
- K071164: Life+Cel Battery (2007), 0 descendants of its own

## Indications for use
To power the functions of various devices for which batteries or battery packs are configured. Since rechargeable batteries and battery packs arc "device specilic" and are designed to operate and fit into the equipment tor which Lhey were manufactured, only qualified personnel should evaluate, test, charge, or install these devices. This battery is shipped only to customers who request a replacement baUery for a particular device or to replace a competitor's replacement battery. Biomedical equipment service professionals therefore know that the intended usc is as a replacement battery.

Source page: https://510kreport.com/device/K032051
Methodology: https://510kreport.com/methodology