Mauna Kea Technologies - FDA 510(k) Cleared Devices
Recent clearances: Cellvizio 100 series system with confocal Miniprobes, Cellvizio I.V.E. system with Confocal Miniprobes, Cellvizio I.V.E. with Confocal Miniprobes
18
Total
18
Cleared
0
Denied
FDA 510(k) Regulatory Record - Mauna Kea Technologies Neurology ✕
1 devices