PRESSURE MANOMETER— 510(k) K110119

Substantially Equivalent

Neoforce Group, Inc.

FDA 510(k) clearance K110119 for PRESSURE MANOMETER, Substantially Equivalent on 2011-06-10. Applicant: Neoforce Group, Inc.. Device class: 2.

Clearance details

Applicant: Neoforce Group, Inc.
Product code: Code CAP
Device class: Class 2
Regulation: 21 CFR 868.2600
Advisory panel: Anesthesiology
Date received: 2011-01-18
Decision date: 2011-06-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ivyland, PA, 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.