Disposable Pressure Manometer (DPM)— 510(k) K143148

Name: FDA 510(k) clearance K143148
Creator: U.S. Food and Drug Administration
Published: 2015-08-11

Substantially Equivalent

Westmed, Inc.

FDA 510(k) clearance K143148 for Disposable Pressure Manometer (DPM), Substantially Equivalent on 2015-08-11. Applicant: Westmed, Inc.. Device class: 2.

Clearance details

Applicant: Westmed, Inc.
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 2014-11-03
Decision date: 2015-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tucson, AZ, US

Download summary PDF View on FDA.gov ↗

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