meddevicedb.com FDA Device Reference

Electronic Blood Pressure Monitor

K200939 Class II Special
Decision Date
2020-08-20
Sponsor / Applicant
Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.

Technical Specification

510(k) Submission ID K200939
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2020-08-20
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Electronic Blood Pressure Monitor received FDA 510(k) clearance under submission number K200939, sponsored by Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2020-08-20.

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.