meddevicedb.com FDA Device Reference

LifeSignals ECG Remote Monitoring Patch Platform

K200690 Class II Traditional
Decision Date
2020-07-15
Sponsor / Applicant
Lifesignals, Inc.

Technical Specification

510(k) Submission ID K200690
Product Code DRG
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2910
Decision Date 2020-07-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LifeSignals ECG Remote Monitoring Patch Platform received FDA 510(k) clearance under submission number K200690, sponsored by Lifesignals, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2020-07-15.

Classification & Regulation

This clearance is catalogued under FDA product code DRG and 21 CFR 870.2910, within the Cardiovascular review panel as a Class II device.