# Lifeline Systems, Inc.

- Location (FDA's records): Walker, MI
- FDA decisions: 4 (1983–2010): 4 510(k) clearances
- Product codes: ILQ (1), DSI (1), DXN (1), DRG (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Hewlett-Packard Co.: 1 (https://510kreport.com/company/hewlett-packard)
- Honeywell Hommed, LLC: 1 (https://510kreport.com/company/honeywell-hommed)

## Firms that cite its devices most
- Visicu, Inc.: 1 (https://510kreport.com/company/visicu)

## Its most-cited devices
- K103214: M3810A Philips Telemonitoring System with Edevice BRIDGED130 (2010), cited by 1

## Recent decisions
- K103214: M3810A Philips Telemonitoring System with Edevice BRIDGED130 (Dec 1, 2010)
- K914103: Lifeline (R) Personal Response System (Sep 27, 1991)
- K834441: Blood Pressure Monitor BP600X (May 21, 1984)
- K831638: Single Bed Arrhythmia Monitor AM500 (Nov 14, 1983)

Source page: https://510kreport.com/company/lifeline-systems