RX02 Plus Oxygen Concentrator

FDA 510(k) K860060 · The John Bunn Co.

Substantially Equivalent

510(k) numberK860060

Submission

Device name
RX02 Plus Oxygen Concentrator
Applicant
The John Bunn Co.
Tonawanda, NY, US
Received
January 6, 1986
Decision date
February 5, 1986
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

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More from Devilbiss Healthcare, LLC

510(k)DeviceDecision
K900854John Bunn: Medix Compact TravellerBTT · Traditional 04/23/1990SE
K883216Bunn Model 50 Oxygen Flow ControllerNFB · Traditional 08/18/1988SE
K873071Bunn Concentrator Model 2100 SeriesCAW · Traditional 09/15/1987SE
K870094Bunn Model 530 AspiratorBTA · Traditional 03/06/1987SE
K861435Bunn Concentrator Model 2011 with Demand ValveCAW · Traditional 11/07/1986SE
K861199Bunn Model 22 Oxygen Flow ControllerNFB · Traditional 08/26/1986SE
K862628Bunn Model 510 Medication CompressorBTI · Traditional 08/07/1986SE
K855208Bunn Lite Oxygen ConcentratorCAW · Traditional 02/21/1986SE
K843811Bunn 3001 Oxygen ConcentratorCAW · Traditional 10/04/1984SE
K841102Bunn 1000 Oxygen ConcentratorCAW · Traditional 04/13/1984SE

Questions and answers

When was RX02 Plus Oxygen Concentrator cleared by the FDA?

RX02 Plus Oxygen Concentrator (K860060) received a 510(k) decision of Substantially Equivalent on February 5, 1986, 30 days after the submission was received.

What is the product code of K860060?

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