# Lifepak 8

> Active: United States. Medical device record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/devices/lifepak-8-ldd>
- Manufacturer: [Physio-Control Corp.](https://devicerts.com/manufacturers/physio-control-inc) (United States)
- Name in the registry: LIFEPAK 8
- Device class: Class II (US FDA)
- FDA product code: LDD

## Overview

*AI-generated summary, 2026-09-23. Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data is the record.*

The Lifepak 8 is a low-energy DC defibrillator that includes paddles for cardiac resuscitation. It is designed to provide diagnostic-quality ECG recording and features both demand and non-demand pacing capabilities.

This device is regulated as a Class 2 medical device under regulation number 870.5300. It has received FDA 510(k) clearance through a traditional submission process.

## Registrations and authorizations

- **510(k)** · FDA 510(k) · United States · K842624 · decision 1984-10-18 · decision SESE · status: Active

## Recalls

No recall on record.

## Identifiers

- 510(k) Number: K842624 [FDA 510(k)]
- FDA product code: LDD [FDA 510(k)]

## Classification

- Device class: Class II [FDA 510(k)]
- Regulation: 21 CFR Part 870.5300 [FDA 510(k)]
- Advisory committee: Cardiovascular [FDA 510(k)]
- FDA decision: SESE [FDA 510(k)]

## Source and citation

- Cite as: Lifepak 8, Physio-Control Corp. deviCERTS medical device catalogue. https://devicerts.com/devices/lifepak-8-ldd (data as of 2026-11-15).
- Data sources: [FDA 510(k)](https://open.fda.gov/apis/device/510k/)
- Registry records last synced: 2026-10-22
- Statuses computed as of: 2026-11-15
- JSON: <https://devicerts.com/devices/lifepak-8-ldd.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/devices/lifepak-8-ldd
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.