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FDA 510(k)

OX-GEN FLEXIBLE O2 GENERATION SYSTEM, MODEL 6-OX-03

K-Number: K033863 · 2005-08-22

ApplicantOx-Gen, Inc.
Decision Date2005-08-22
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OX-GEN FLEXIBLE O2 GENERATION SYSTEM, MODEL 6-OX-03 is the device name listed in this FDA 510(k) record. The listed applicant is Ox-Gen, Inc.. It received FDA 510(k) clearance on 2005-08-22 under 510(k) number K033863. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OX-GEN FLEXIBLE O2 GENERATION SYSTEM, MODEL 6-OX-03?

OX-GEN FLEXIBLE O2 GENERATION SYSTEM, MODEL 6-OX-03 is a medical device that received FDA 510(k) clearance on 2005-08-22. The listed applicant is Ox-Gen, Inc.. The 510(k) number is K033863.

When did OX-GEN FLEXIBLE O2 GENERATION SYSTEM, MODEL 6-OX-03 receive FDA 510(k) clearance?

OX-GEN FLEXIBLE O2 GENERATION SYSTEM, MODEL 6-OX-03 received FDA 510(k) clearance on 2005-08-22, under 510(k) number K033863.

Who is the listed applicant for OX-GEN FLEXIBLE O2 GENERATION SYSTEM, MODEL 6-OX-03?

The FDA 510(k) record lists Ox-Gen, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OX-GEN FLEXIBLE O2 GENERATION SYSTEM, MODEL 6-OX-03?

The FDA product code for OX-GEN FLEXIBLE O2 GENERATION SYSTEM, MODEL 6-OX-03 is CAW.

Related Clinical Trials

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.

Related Devices (Code: CAW)

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.

Official Source

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