Medical Device Manufacturer · FR , Conflans Sainte Honorine

Integral Process Sas

2 submissions · 2 cleared · Since 2010
2
Total
2
Cleared
0
Denied

Integral Process Sas — FDA 510(k) Submissions

Integral Process Sas has submitted 2 FDA 510(k) premarket notifications since 2010, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrode, Electrocardiograph, Cable, Transducer And Electrode, Patient, (including Connector) . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
Filters
Filter by Specialty
All2 Cardiovascular 2