Tanscu O2

FDA 510(k) K090681 · Electrochemical Oxygen Concepts, Inc.

Substantially Equivalent

510(k) numberK090681

Submission

Device name
Tanscu O2
Applicant
Electrochemical Oxygen Concepts, Inc.
Lake Bluff, IL, US
Received
March 16, 2009
Decision date
August 12, 2009
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 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
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
K022028VX-400 Topical Hyperbaric Oxygen ChamberKPJ · Traditional Vascular One, Inc.12/17/2002SE
K020466Hec 1000KPJ · Traditional Metro Medical Equipment, Inc.05/08/2002SE

Questions and answers

When was Tanscu O2 cleared by the FDA?

Tanscu O2 (K090681) received a 510(k) decision of Substantially Equivalent on August 12, 2009, 149 days after the submission was received.

What is the product code of K090681?

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