meddevicedb.com FDA Device Reference

VS-800 VITAL SIGNS MONITOR

K063055 Class II Traditional
Decision Date
2006-12-21
Sponsor / Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Technical Specification

510(k) Submission ID K063055
Product Code MWI
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2300
Decision Date 2006-12-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VS-800 VITAL SIGNS MONITOR received FDA 510(k) clearance under submission number K063055, sponsored by Shenzhen Mindray Bio-Medical Electronics Co., 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 2006-12-21.

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.