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Modified Digital Blood Pressure/Pulse Meter

by Vestra-Subco, Inc.

510(k) K872144

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK872144 Date29 Jul 1987ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
DXQ
Device Class
Class II
Regulation
21 CFR Part 870.1120
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 27 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 Modified Digital Blood Pressure/Pulse Meter is a blood pressure cuff designed to measure blood pressure and pulse rate. It functions as a diagnostic device for cardiovascular monitoring.

This device is identified by K-number K872144 and has received FDA 510(k) clearance. It is classified under the cardiovascular medical specialty and is regulated under 21 CFR 870.1120.

Questions

AI-generated answers, 27 Sep 2026

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

  • What is the primary function of the Modified Digital Blood Pressure/Pulse Meter?

    This device is designed to serve as a cardiovascular diagnostic tool. It is specifically engineered to measure both a patient's blood pressure and their pulse rate.

  • Is this device cleared for use by regulatory authorities?

    Yes, the Modified Digital Blood Pressure/Pulse Meter has received FDA 510(k) clearance under K-number K872144. It is regulated under 21 CFR 870.1120.

  • How is this device classified within the medical field?

    The device is classified under the cardiovascular medical specialty. It is categorized by the FDA under product code DXQ and is reviewed by the cardiovascular advisory committee.