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A & D MEDICAL UA-767BT DIGITAL BLOOD PRESSURE MONITOR

K040371 Class II Special
Decision Date
2004-05-19
Sponsor / Applicant
A&D Engineering, Inc.

Technical Specification

510(k) Submission ID K040371
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2004-05-19
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

A & D MEDICAL UA-767BT DIGITAL BLOOD PRESSURE MONITOR received FDA 510(k) clearance under submission number K040371, sponsored by A&D Engineering, 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 2004-05-19.

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.