AMBULATORY BLOOD PRESSURE MONITOR, MDL# 5100-01— 510(k) K925899

Name: FDA 510(k) clearance K925899
Creator: U.S. Food and Drug Administration
Published: 1993-05-21

Substantially Equivalent

Welch Allyn, Inc.

FDA 510(k) clearance K925899 for AMBULATORY BLOOD PRESSURE MONITOR, MDL# 5100-01, Substantially Equivalent on 1993-05-21. Applicant: Welch Allyn, Inc.. Device class: 2.

Clearance details

Applicant: Welch Allyn, Inc.
Product code: Code DSK
Device class: Class 2
Regulation: 21 CFR 870.1110
Advisory panel: Cardiovascular
Date received: 1992-11-20
Decision date: 1993-05-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Skaneateles Falls, NY, US

Download summary PDF View on FDA.gov ↗

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