Prolira B.V. - FDA 510(k) Cleared Devices
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.
510(k) submissions have been managed by Corolla Clin/Reg Consulting as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Prolira B.V.
2 devices