meddevicedb.com FDA Device Reference

EMT-102 CARDIAC MONITOR

K870049 Class II Traditional
Decision Date
1987-04-22
Sponsor / Applicant
Evergreen Medical Technologies, Inc.

Technical Specification

510(k) Submission ID K870049
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 1987-04-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMT-102 CARDIAC MONITOR received FDA 510(k) clearance under submission number K870049, sponsored by Evergreen Medical Technologies, 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 1987-04-22.

Classification & Regulation

This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.