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FDA 510(k)

Kingon P2 Oxygen Concentrator

K-Number: K190304 · 2020-02-29

ApplicantQingdao Kingon Medical Science and Technology Co.
Decision Date2020-02-29
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Kingon P2 Oxygen Concentrator is a medical device manufactured by Qingdao Kingon Medical Science and Technology Co.. It received FDA 510(k) clearance on 2020-02-29 under approval number K190304. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Kingon P2 Oxygen Concentrator?

Kingon P2 Oxygen Concentrator is a medical device that received FDA 510(k) clearance on 2020-02-29. It is manufactured by Qingdao Kingon Medical Science and Technology Co.. The 510(k) number is K190304.

When was Kingon P2 Oxygen Concentrator approved by the FDA?

Kingon P2 Oxygen Concentrator received FDA 510(k) clearance on 2020-02-29, under approval number K190304.

What company makes Kingon P2 Oxygen Concentrator?

Kingon P2 Oxygen Concentrator is manufactured by Qingdao Kingon Medical Science and Technology Co..

What is the FDA product code for Kingon P2 Oxygen Concentrator?

The FDA product code for Kingon P2 Oxygen Concentrator is CAW.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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