Medical Device Manufacturer · US , North Andover , MA

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

1 submissions · 1 cleared · Since 2000
1
Total
1
Cleared
0
Denied

Oni, Inc. has 1 FDA 510(k) cleared medical devices. Based in North Andover, US.

Historical record: 1 cleared submissions from 2000 to 2000. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Oni, Inc.
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