Maxter Catheters is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Maxter Catheters - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Maxter Catheters has 1 FDA 510(k) cleared medical devices. Based in Marseille, FR.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Maxter Catheters Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Maxter Catheters
1 devices