Lifewatch Technologies , Ltd. is one of 489 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Lifewatch Technologies , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Vital Signs Patch System, ECG Mini System Continuous ECG Monitor and Arrhythmia Detector, CG-6108 ACT-3L Continuous ECG Monitor and Arrhythmia Detector
4
Total
4
Cleared
0
Denied
Lifewatch Technologies , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Rehovot, IL.
Historical record: 4 cleared submissions from 2014 to 2016. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Lifewatch Technologies , Ltd. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Life Watch and Biologics Consulting Group, Inc..
FDA 510(k) Regulatory Record - Lifewatch Technologies , Ltd.
4 devices
Cleared
Feb 05, 2016
Vital Signs Patch System
Cardiovascular
214d
Cleared
Jan 15, 2016
ECG Mini System Continuous ECG Monitor and Arrhythmia Detector
Cardiovascular
247d
Cleared
Sep 11, 2015
CG-6108 ACT-3L Continuous ECG Monitor and Arrhythmia Detector
Cardiovascular
291d
Cleared
Dec 19, 2014
VITAL SIGNS PATCH SYSTEM (IN SHORT VSP)
Cardiovascular
504d