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FDA 510(k)

OxyGo Portable Oxygen Concentrator (1400-7000)

K-Number: K252407 · 2026-04-23

ApplicantMv Life, LLC
Decision Date2026-04-23
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OxyGo Portable Oxygen Concentrator (1400-7000) is a medical device manufactured by Mv Life, LLC. It received FDA 510(k) clearance on 2026-04-23 under approval number K252407. 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 OxyGo Portable Oxygen Concentrator (1400-7000)?

OxyGo Portable Oxygen Concentrator (1400-7000) is a medical device that received FDA 510(k) clearance on 2026-04-23. It is manufactured by Mv Life, LLC. The 510(k) number is K252407.

When was OxyGo Portable Oxygen Concentrator (1400-7000) approved by the FDA?

OxyGo Portable Oxygen Concentrator (1400-7000) received FDA 510(k) clearance on 2026-04-23, under approval number K252407.

What company makes OxyGo Portable Oxygen Concentrator (1400-7000)?

OxyGo Portable Oxygen Concentrator (1400-7000) is manufactured by Mv Life, LLC.

What is the FDA product code for OxyGo Portable Oxygen Concentrator (1400-7000)?

The FDA product code for OxyGo Portable Oxygen Concentrator (1400-7000) is CAW.

Related Clinical Trials

NCT06868979 Optical Imaging in X-linked Disorders. RECRUITING NCT07512687 Titrated Ambulatory Oxygen in Fibrotic ILD and COPD With Isolated Exertional Hypoxemia NOT_YET_RECRUITING

Related Devices (Code: 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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