Medical Device Manufacturer · IT , Cologno Monzese

Wise S.R.L. - FDA 510(k) Cleared Devices

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

Wise S.R.L. has 1 FDA 510(k) cleared medical devices. Based in Cologno Monzese, IT.

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

Browse the FDA 510(k) cleared devices submitted by Wise S.R.L. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Decus Biomedical as regulatory consultant.

FDA 510(k) Regulatory Record - Wise S.R.L.
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