meddevicedb.com FDA Device Reference

BS-200 CHEMISTRY ANALYZER, MODE BS-200

K072018 Class II Traditional
Decision Date
2008-02-01
Sponsor / Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Technical Specification

510(k) Submission ID K072018
Product Code CFR
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2008-02-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BS-200 CHEMISTRY ANALYZER, MODE BS-200 received FDA 510(k) clearance under submission number K072018, sponsored by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2008-02-01.

Classification & Regulation

This clearance is catalogued under FDA product code CFR and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.