Medical Device Manufacturer · US , San Diego , CA

Axis - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1999
1
Total
1
Cleared
0
Denied

Axis has 1 FDA 510(k) cleared medical devices. Based in San Diego, US.

Historical record: 1 cleared submissions from 1999 to 1999. Primary specialty: Chemistry.

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

FDA 510(k) cleared devices by Axis

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