Prolaio, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Prolaio, Inc. has 1 FDA 510(k) cleared medical devices. Based in Chicago, US.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Prolaio, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Prolaio, Inc.
1 devices