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YUWELL® Electronic Blood Pressure Monitor (YE630CR)

K252779 Class II Traditional
Decision Date
2026-03-05
Sponsor / Applicant
Jiangsu Yuyue Medical Equipment & Supply Co., Ltd.

Technical Specification

510(k) Submission ID K252779
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2026-03-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

YUWELL® Electronic Blood Pressure Monitor (YE630CR) received FDA 510(k) clearance under submission number K252779, sponsored by Jiangsu Yuyue Medical Equipment & Supply 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 2026-03-05.

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.