meddevicedb.com FDA Device Reference

HEALTHVIEW ECG MANAGER

K123466 Class II Traditional
Decision Date
2012-12-20
Sponsor / Applicant
Lumedx

Technical Specification

510(k) Submission ID K123466
Product Code DQK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1425
Decision Date 2012-12-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEALTHVIEW ECG MANAGER received FDA 510(k) clearance under submission number K123466, sponsored by Lumedx. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2012-12-20.

Classification & Regulation

This clearance is catalogued under FDA product code DQK and 21 CFR 870.1425, within the Cardiovascular review panel as a Class II device.