A&D TM-2421/2021 AMBULATORY BLOOD PRESSURE MONITOR— 510(k) K914273

Name: FDA 510(k) clearance K914273
Creator: U.S. Food and Drug Administration
Published: 1993-02-09

Substantially Equivalent

A&D Engineering, Inc.

FDA 510(k) clearance K914273 for A&D TM-2421/2021 AMBULATORY BLOOD PRESSURE MONITOR, Substantially Equivalent on 1993-02-09. Applicant: A&D Engineering, Inc.. Device class: 2.

Clearance details

Applicant: A&D Engineering, Inc.
Product code: Code DSK
Device class: Class 2
Regulation: 21 CFR 870.1110
Advisory panel: Cardiovascular
Date received: 1991-09-24
Decision date: 1993-02-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Milpitas, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DSK

view all

K231586 — Endophys Blood Pressure Monitor model BPM-302023-11-03
K160945 — Endophys Blood Pressure Monitor2016-09-26
K152582 — CORE FM System, Patient Interface Module (OPIM), Hemodynamic Converter Box2015-12-03
K141615 — ENDOPHYS BLOOD PRESSURE MONITOR2015-01-07
K080670 — MODIFICATION TO SPHYGMOCOR CARDIOVASCULAR MANAGEMENT SYSTEM2008-04-23

More clearances from A&D Engineering, Inc.

view all

Data sourced from openFDA. This site is unofficial and independent of the FDA.