meddevicedb.com FDA Device Reference

Med-link Reusable Blood Pressure Cuff, Med-link Disposable Blood Pressure Cuff

K160530 Class II Traditional
Decision Date
2016-11-28
Sponsor / Applicant
Shenzhen Med-Link Electronics Tech Co., Ltd.

Technical Specification

510(k) Submission ID K160530
Product Code DXQ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1120
Decision Date 2016-11-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Med-link Reusable Blood Pressure Cuff, Med-link Disposable Blood Pressure Cuff received FDA 510(k) clearance under submission number K160530, sponsored by Shenzhen Med-Link Electronics Tech 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 2016-11-28.

Classification & Regulation

This clearance is catalogued under FDA product code DXQ and 21 CFR 870.1120, within the Cardiovascular review panel as a Class II device.