Integral Process Sas is one of 289 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Integral Process Sas - FDA 510(k) Cleared Devices
Recent clearances: ECG multi leads and IP-SET trunk cable, Monobloc ECG cable, SpO2 sensors and IBP transducers interface cable, ECG leadwire for INTEGRAL PROCESS trunk cables, ECG leadwire for original truk cables, IP-SET
2
Total
2
Cleared
0
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.
510(k) submissions have been managed by Tuv Rheinland of North America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Integral Process Sas
2 devices