meddevicedb.com FDA Device Reference

Upper Arm Blood pressure monitor (BP7155D)

K261929 Class II Special
Decision Date
2026-09-10
Sponsor / Applicant
OMRON Healthcare, Inc.

Technical Specification

510(k) Submission ID K261929
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2026-09-10
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Upper Arm Blood pressure monitor (BP7155D) received FDA 510(k) clearance under submission number K261929, sponsored by OMRON Healthcare, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2026-09-10.

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.