meddevicedb.com FDA Device Reference

PC ECG 1200

K000404 Class II Traditional
Decision Date
2000-11-22
Sponsor / Applicant
Norav Medical , Ltd.

Technical Specification

510(k) Submission ID K000404
Product Code MWI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2000-11-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PC ECG 1200 received FDA 510(k) clearance under submission number K000404, sponsored by Norav Medical , 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 2000-11-22.

Classification & Regulation

This clearance is catalogued under FDA product code MWI and 21 CFR 870.2300, within the Cardiovascular review panel as a Class II device.