Medical Device Manufacturer · NL , Utrecht

Prolira B.V. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2023
2
Total
2
Cleared
0
Denied

Prolira B.V. has 2 FDA 510(k) cleared medical devices. Based in Utrecht, NL.

Last cleared in 2023. Active since 2023. Primary specialty: Neurology.

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

FDA 510(k) cleared devices by Prolira B.V.

2 devices
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All2 Neurology 2