Portable Oxygen Concentrator (Model: P2-E7, P2-E)

FDA 510(k) K223379 · Qingdao Kingon Medical Science and Technology Co., Ltd.

Substantially Equivalent

510(k) numberK223379

Submission

Device name
Portable Oxygen Concentrator (Model: P2-E7, P2-E)
Applicant
Qingdao Kingon Medical Science and Technology Co., Ltd.
Qingdao Free Trade Zone, CN
Received
November 7, 2022
Decision date
June 22, 2023
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

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More from Devilbiss Healthcare, LLC

510(k)DeviceDecision
K251764Oxygen Concentrator-P2-O5ECAW · Traditional 12/22/2025SE
K242718Portable Oxygen Concentrator (P2-TOC)CAW · Traditional 02/28/2025SE
K230702Portable Oxygen Concentrator (Model: P2-S4, P2-S3,P2-K4,P2-K3)CAW · Traditional 10/18/2023SE
K210371Portable Oxygen Concentrator, model: P2-E6CAW · Traditional 06/03/2022SE
K190304Kingon P2 Oxygen ConcentratorCAW · Traditional 02/29/2020SE

Questions and answers

When was Portable Oxygen Concentrator (Model: P2-E7, P2-E) cleared by the FDA?

Portable Oxygen Concentrator (Model: P2-E7, P2-E) (K223379) received a 510(k) decision of Substantially Equivalent on June 22, 2023, 227 days after the submission was received.

What is the product code of K223379?

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