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FDA 510(k)

Oxygen Concentrator

K-Number: K202389 · 2022-04-08

Decision Date2022-04-08
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Oxygen Concentrator is the device name listed in this FDA 510(k) record. The listed applicant is Foshan Mic Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-04-08 under 510(k) number K202389. 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 Oxygen Concentrator?

Oxygen Concentrator is a medical device that received FDA 510(k) clearance on 2022-04-08. The listed applicant is Foshan Mic Medical Technology Co., Ltd.. The 510(k) number is K202389.

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

Oxygen Concentrator received FDA 510(k) clearance on 2022-04-08, under 510(k) number K202389.

Who is the listed applicant for Oxygen Concentrator?

The FDA 510(k) record lists Foshan Mic Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Oxygen Concentrator?

The FDA product code for Oxygen Concentrator is CAW.

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