Medical Device Manufacturer · US , Riverside , CA

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

3 submissions · 3 cleared · Since 1987
3
Total
3
Cleared
0
Denied

Nunc, Inc. has 3 FDA 510(k) cleared medical devices. Based in Riverside, US.

Historical record: 3 cleared submissions from 1987 to 1987. Primary specialty: Pathology.

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

FDA 510(k) Regulatory Record - Nunc, Inc.
3 devices
1-3 of 3
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