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A&D MEDICAL UB-543 DIGITAL BLOOD PRESSURE MONITOR

K141179 Class II Special
Decision Date
2014-06-27
Sponsor / Applicant
A & D Co., Ltd.

Technical Specification

510(k) Submission ID K141179
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2014-06-27
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

A&D MEDICAL UB-543 DIGITAL BLOOD PRESSURE MONITOR received FDA 510(k) clearance under submission number K141179, sponsored by A & D 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 2014-06-27.

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.