Medical Device Manufacturer · FR , Conflans Sainte Honorine

Integral Process Sas - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2010

Total

Cleared

Denied

Integral Process Sas has 2 FDA 510(k) cleared medical devices. Based in Conflans Sainte Honorine, FR.

Historical record: 2 cleared submissions from 2010 to 2017. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Integral Process Sas Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Integral Process Sas

2 devices

1-2 of 2