Medical Device Manufacturer · US , Auburn Hills , MI

Oxus, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2017
2
Total
2
Cleared
0
Denied

Oxus, Inc. has 2 FDA 510(k) cleared medical devices. Based in Auburn Hills, US.

Last cleared in 2023. Active since 2017. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Oxus, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Oxus, Inc. % Promedic, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Oxus, Inc.
2 devices
1-2 of 2
Cleared May 31, 2023
Oxus Sieve Beds
K211056 · CAW
Anesthesiology · 782d
Cleared May 24, 2017
GCE Zen-O Portable Oxygen Concentrator
K162433 · CAW
Anesthesiology · 266d
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