Oxlife Oxygen Concentrators

FDA 510(k) K955549 · Oxlife, Inc.

Substantially Equivalent

510(k) numberK955549

Submission

Device name
Oxlife Oxygen Concentrators
Applicant
Oxlife, Inc.
Cape Coral, FL, US
Received
December 5, 1995
Decision date
March 15, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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
K080082Oxlife Independence Oxygen ConcentratorsCAW · Traditional 04/16/2008SE
K060922Oxlife Freedom Five Oxygen Concentrators, Model KXF5CAW · Special 05/30/2006SE
K971964Oxlife Excell Oxygen ConcentratorsCAW · Traditional 08/15/1997SE
K933081Oxlife Oxygen ConcentratorCAW · Traditional 11/01/1994SE

Questions and answers

When was Oxlife Oxygen Concentrators cleared by the FDA?

Oxlife Oxygen Concentrators (K955549) received a 510(k) decision of Substantially Equivalent on March 15, 1996, 101 days after the submission was received.

What is the product code of K955549?

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