Medical Device Manufacturer · US , Oklahoma City , OK

Xironetic, LLC - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022
1
Total
1
Cleared
0
Denied

Xironetic, LLC has 1 FDA 510(k) cleared medical devices. Based in Oklahoma City, US.

Last cleared in 2022. Active since 2022. Primary specialty: Radiology.

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

510(k) submissions have been managed by Paladin Medical, Inc. as regulatory consultant.

FDA 510(k) Regulatory Record - Xironetic, LLC
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