RESPO2 Oxygen Concentrator

FDA 510(k) K802426 · Mada Medical Products, Inc.

Substantially Equivalent

510(k) numberK802426

Submission

Device name
RESPO2 Oxygen Concentrator
Applicant
Mada Medical Products, Inc.
Walker, MI, US
Received
October 6, 1980
Decision date
October 23, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CAW – Generator, Oxygen, Portable
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5440
Specialty
Anesthesiology

Other 510(k)s with product code CAW

510(k)DeviceApplicantDecision
K260171Portable Oxygen Concentrator (PO1 5B, PO1 6B)CAW · Traditional BMC Medical Co., Ltd.08/14/2026SE
K252399Portable Oxygen ConcentratorCAW · Traditional Honsun (Nantong) Co., Ltd.06/17/2026SE
K252965Oxygen Concentrator (OX-5A, OX-5C)CAW · Traditional Oxytek Medical Technology Co., Ltd.05/29/2026SE
K252407OxyGo Portable Oxygen Concentrator (1400-7000)CAW · Traditional Mv Life, LLC04/23/2026SE
K253549DeVilbiss 5 Liter Oxygen Concentrator (555)CAW · Traditional Devilbiss Healthcare, LLC03/26/2026SE
K251534Oxygen Concentrator (J10A)CAW · Traditional Foshan Kycare Medical Equipment Co., Ltd.12/29/2025SE
K252616Portable oxygen concentrator (JLO-190P)CAW · Traditional Shenzhen Homed Medical Device Co., Ltd.12/22/2025SE
K251764Oxygen Concentrator-P2-O5ECAW · Traditional Qingdao Kingon Medical Science and Technology…12/22/2025SE
K252268V series portable oxygen concentrator (V5, V5C, V6, V6C)CAW · Traditional Shenzhen Harveymed Technology Co., Ltd.12/16/2025SE
K250805DeVilbiss PulmO2 10-Liter Oxygen Concentrator (1060AW)CAW · Traditional Devilbiss Healthcare, LLC12/09/2025SE

More from Devilbiss Healthcare, LLC

510(k)DeviceDecision
K003862Mada WheelchairsIOR · Traditional 01/12/2001SE
K002943Wheelchair, Mechanical Series Model 3100IOR · Traditional 10/23/2000SE
K950777Oxygen RegulatorCAN · Traditional 04/14/1995SE
K930949VoyageCAF · Traditional 06/01/1993SE
K930947PromenadeCAF · Traditional 06/01/1993SE
K921611Madavac 190BTA · Traditional 09/09/1992SE
K850754Medajet XL - Jet InjectorKZE · Traditional 12/10/1985SE

Questions and answers

When was RESPO2 Oxygen Concentrator cleared by the FDA?

RESPO2 Oxygen Concentrator (K802426) received a 510(k) decision of Substantially Equivalent on October 23, 1980, 17 days after the submission was received.

What is the product code of K802426?

The FDA product code is CAW – Generator, Oxygen, Portable, a Class II (moderate risk) device regulated under 21 CFR 868.5440.