meddevicedb.com FDA Device Reference

Wrist Type Blood Pressure Monitor (W05,W1101L)

K230409 Class II Traditional
Decision Date
2023-08-25
Sponsor / Applicant
Shenzhen Jamr Technology Co., Ltd.

Technical Specification

510(k) Submission ID K230409
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2023-08-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Wrist Type Blood Pressure Monitor (W05,W1101L) received FDA 510(k) clearance under submission number K230409, sponsored by Shenzhen Jamr Technology 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 2023-08-25.

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.