Medical Device Manufacturer · US , Lubbock , TX

Genesis Air, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2023
1
Total
1
Cleared
0
Denied

Genesis Air, Inc. has 1 FDA 510(k) cleared medical devices. Based in Lubbock, US.

Last cleared in 2023. Active since 2023. Primary specialty: General Hospital.

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

510(k) submissions have been managed by Sterling Medical Devices as regulatory consultant.

FDA 510(k) Regulatory Record - Genesis Air, Inc.
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