meddevicedb.com FDA Device Reference

EHC 400 DESKTOP PATIENT STATION, EHC 600 CORE PROVIDER STATION

K000237 Class II Traditional
Decision Date
2000-06-13
Sponsor / Applicant
Cybercare, Inc.

Technical Specification

510(k) Submission ID K000237
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2000-06-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EHC 400 DESKTOP PATIENT STATION, EHC 600 CORE PROVIDER STATION received FDA 510(k) clearance under submission number K000237, sponsored by Cybercare, 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 2000-06-13.

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.