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FDA 510(k)

EZ-OX PLUS

K-Number: K053117 · 2006-04-10

ApplicantAir Liquide Healthcare America
Decision Date2006-04-10
Product CodeECX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EZ-OX PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Air Liquide Healthcare America. It received FDA 510(k) clearance on 2006-04-10 under 510(k) number K053117. The device is classified under product code ECX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZ-OX PLUS?

EZ-OX PLUS is a medical device that received FDA 510(k) clearance on 2006-04-10. The listed applicant is Air Liquide Healthcare America. The 510(k) number is K053117.

When did EZ-OX PLUS receive FDA 510(k) clearance?

EZ-OX PLUS received FDA 510(k) clearance on 2006-04-10, under 510(k) number K053117.

Who is the listed applicant for EZ-OX PLUS?

The FDA 510(k) record lists Air Liquide Healthcare America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EZ-OX PLUS?

The FDA product code for EZ-OX PLUS is ECX.

Related Devices (Code: ECX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K161179Intelli-OxAir Liquide Healthcare America CorporationK161472Walk-O2-BoutEssex Industries, Inc.K153518Medipure Oxygen-LC SystemPraxair Distribution, Incorporated.K101792LIV LINDE INTERGRATED VALVE-PORTABLE OXYGEN SYSTEM, MODEL M706Linde Gas North America, LLCK063354LINDE INTEGRATED VALVE (LIV)Linde Gas TherapeuticsK062300OX-SOX, MODEL C, D, E,Pattient Safety Innovations, Llp

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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