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# Medi-Lynx’s PocketECG Cardiac Rehab System Cleared
- URL: https://www.fdaweb.com/medi-lynxs-pocketecg-cardiac-rehab-system-cleared/
- Published: 2018-07-23T12:00:00.000Z
- Updated: 2026-09-15T00:21:05.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5141934

FDA has cleared a Medi-Lynx Cardiac Monitoring 510(k) for the PocketECG Cardiac Rehabilitation System, a mobile cardiac rehabilitation designed to provide ECG monitoring and automated arrhythmia detection during rehabilitation training. The smartphone-sized device is intended to monitor a patient’s heart rhythm and heart rate during rehabilitation exercises to safely guide the intensity and duration of workouts in real-time. It transmits the full disclosure ECG signal classifying every heartbeat to automatically detect abnormalities and arrhythmia, according to the company. Additionally, a built-in accelerometer allows clinicians to analyze the impact of physical activity on heart rate. All data are streamed to a secure online clinician portal and to a cardiac monitoring center for constant monitoring, evaluation, and urgent notifications, it says.