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A&D UA-767PC Digital Blood Pressure Monitor

by A&D Engineering, Inc.

510(k) K982481

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 24 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK982481 Date25 Sep 1998ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 24 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

Full name
A&D Medical Ua-767PC Digital Blood Pressure Monitor
510(k) Number
FDA Product Code
DXN
Device Class
Class II
Regulation
21 CFR Part 870.1130
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 18 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The A&D UA-767PC is an upper arm blood pressure monitor designed for measuring systolic and diastolic blood pressure. It operates as an automated oscillometric device, providing accurate readings for clinical or home use by inflating a cuff around the upper arm and detecting arterial pulsations.

This device is supplied as a reusable, non-sterile medical instrument intended for single-patient use per session. It features data storage for up to 280 measurements and RS-232C connectivity for external data transfer. Authorized under FDA 510(k) clearance (K982481), it adheres to traditional review standards and is classified under product code DXN.

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