NeumoFilt Ergo/Neumo Filt BiteOn— 510(k) K142303

Name: FDA 510(k) clearance K142303
Creator: U.S. Food and Drug Administration
Published: 2014-11-20

Substantially Equivalent

Medical Respiratory Devices S.L.

FDA 510(k) clearance K142303 for NeumoFilt Ergo/Neumo Filt BiteOn, Substantially Equivalent on 2014-11-20. Applicant: Medical Respiratory Devices S.L.. Device class: 2.

Clearance details

Applicant: Medical Respiratory Devices S.L.
Product code: Code BZG
Device class: Class 2
Regulation: 21 CFR 868.1840
Advisory panel: Anesthesiology
Date received: 2014-08-18
Decision date: 2014-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Coslada(Madrid), ES

Download summary PDF View on FDA.gov ↗

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