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FDA 510(k)

Kingon P2 Oxygen Concentrator

K-Number: K190304 · 2020-02-29

Decision Date2020-02-29
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Kingon P2 Oxygen Concentrator is the device name listed in this FDA 510(k) record. The listed applicant is Qingdao Kingon Medical Science and Technology Co.. It received FDA 510(k) clearance on 2020-02-29 under 510(k) 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. The listed applicant is Qingdao Kingon Medical Science and Technology Co.. The 510(k) number is K190304.

When did Kingon P2 Oxygen Concentrator receive FDA 510(k) clearance?

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

Who is the listed applicant for Kingon P2 Oxygen Concentrator?

The FDA 510(k) record lists Qingdao Kingon Medical Science and Technology Co. as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Qingdao Kingon Medical Science and Technology Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: CAW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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