Kingon P2 Oxygen Concentrator

FDA 510(k) K190304 · Qingdao Kingon Medical Science and Technology Co.

Substantially Equivalent

510(k) numberK190304

Submission

Device name
Kingon P2 Oxygen Concentrator
Applicant
Qingdao Kingon Medical Science and Technology Co.
Qingdao, CN
Received
February 12, 2019
Decision date
February 29, 2020
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

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K251764Oxygen Concentrator-P2-O5ECAW · Traditional 12/22/2025SE
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K230702Portable Oxygen Concentrator (Model: P2-S4, P2-S3,P2-K4,P2-K3)CAW · Traditional 10/18/2023SE
K223379Portable Oxygen Concentrator (Model: P2-E7, P2-E)CAW · Traditional 06/22/2023SE
K210371Portable Oxygen Concentrator, model: P2-E6CAW · Traditional 06/03/2022SE

Questions and answers

When was Kingon P2 Oxygen Concentrator cleared by the FDA?

Kingon P2 Oxygen Concentrator (K190304) received a 510(k) decision of Substantially Equivalent on February 29, 2020, 382 days after the submission was received.

What is the product code of K190304?

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