meddevicedb.com FDA Device Reference

VITAL SIGNS PATCH SYSTEM (IN SHORT VSP)

K132407 Class II Traditional
Decision Date
2014-12-19
Sponsor / Applicant
Lifewatch Technologies , Ltd.

Technical Specification

510(k) Submission ID K132407
Product Code DSI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1025
Decision Date 2014-12-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VITAL SIGNS PATCH SYSTEM (IN SHORT VSP) received FDA 510(k) clearance under submission number K132407, sponsored by Lifewatch Technologies , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2014-12-19.

Classification & Regulation

This clearance is catalogued under FDA product code DSI and 21 CFR 870.1025, within the Cardiovascular review panel as a Class II device.