# Lifewatch Technologies, Ltd.

- Location (FDA's records): Rehovot, IL
- FDA decisions: 4 (2014–2016): 4 510(k) clearances
- Product codes: DSI (4)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Card Guard Scientific Survival, Ltd.: 2 (https://510kreport.com/company/card-guard-scientific-survival)
- Welch Allyn Protocol, Inc.: 1 (https://510kreport.com/company/welch-allyn-protocol)
- Intelesens Limited: 1 (https://510kreport.com/company/intelesens)
- Beijing Choice Electronic Technololgy Co., Ltd.: 1 (https://510kreport.com/company/beijing-choice-electronic-technololgy)

## Firms that cite its devices most
- Lifewatch Services, Inc.: 1 (https://510kreport.com/company/lifewatch-services)

## Its most-cited devices
- K132407: Vital Signs Patch System (in Short VSP) (2014), cited by 1
- K143359: CG-6108 ACT-3L Continuous ECG Monitor and Arrhythmia Detector (2015), cited by 1

## Recent decisions
- K151835: Vital Signs Patch System (Feb 5, 2016)
- K151269: ECG Mini System Continuous ECG Monitor and Arrhythmia Detector (Jan 15, 2016)
- K143359: CG-6108 ACT-3L Continuous ECG Monitor and Arrhythmia Detector (Sep 11, 2015)
- K132407: Vital Signs Patch System (in Short VSP) (Dec 19, 2014)

Source page: https://510kreport.com/company/lifewatch-technologies