VX-400 Topical Hyperbaric Oxygen Chamber

FDA 510(k) K022028 · Vascular One, Inc.

Substantially Equivalent

510(k) numberK022028

Submission

Device name
VX-400 Topical Hyperbaric Oxygen Chamber
Applicant
Vascular One, Inc.
Great Neck, NY, US
Received
June 21, 2002
Decision date
December 17, 2002
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KPJ – Chamber, Oxygen, Topical, Extremity
Device class
Class II (moderate risk)
Regulation
21 CFR 878.5650
Specialty
General, Plastic Surgery

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K190742EPIFLO-28KPJ · Traditional Neogenix, LLC Dba Ogenix12/13/2019SE
K112634Natrox Topical Oxygen Delivery System with IodpKPJ · Traditional Inotec Amd , Ltd.07/03/2012SE
K120764Epiflo(R)KPJ · Special Neogenix, LLC04/27/2012SE
K090681Tanscu O2KPJ · Abbreviated Electrochemical Oxygen Concepts, Inc.08/12/2009SE
K080966Hyper-Box Topical Wound Oxygen SystemKPJ · Traditional Aoti , Ltd.08/06/2008SE
K050156WHS-1000 Wound Healing SystemKPJ · Traditional Iyia Technologies, Inc.06/17/2005SE
K023456Oxybox SystemKPJ · Traditional Oxyfast Corporation02/24/2003SE
K020466Hec 1000KPJ · Traditional Metro Medical Equipment, Inc.05/08/2002SE

Questions and answers

When was VX-400 Topical Hyperbaric Oxygen Chamber cleared by the FDA?

VX-400 Topical Hyperbaric Oxygen Chamber (K022028) received a 510(k) decision of Substantially Equivalent on December 17, 2002, 179 days after the submission was received.

What is the product code of K022028?

The FDA product code is KPJ – Chamber, Oxygen, Topical, Extremity, a Class II (moderate risk) device regulated under 21 CFR 878.5650.