Pentaferte Italia S.R.L. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Pentaferte Italia S.R.L. has 3 FDA 510(k) cleared medical devices. Based in Campli, IT.
Last cleared in 2022. Active since 2017. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Pentaferte Italia S.R.L. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Vygon USA and Pqe US.
3 devices