Medical Device Manufacturer · US , Buffalo , NY

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

1 submissions · 1 cleared · Since 2006

Total

Cleared

Denied

Praesidia S.R.L. has 1 FDA 510(k) cleared medical devices. Based in Buffalo, US.

Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: Orthopedic.

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

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

1 devices

1-1 of 1