Pendracare International, B.V. is one of 5183 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pendracare International, B.V. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Pendracare International, B.V. has 2 FDA 510(k) cleared medical devices. Based in Raleigh, US.
Historical record: 2 cleared submissions from 2012 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Pendracare International, B.V. Filter by specialty or product code using the sidebar.
Pendracare International, B.V. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Aug 12, 2013
CONVEY 7F GUIDING CATHETER, CONVEY 8F GUIDING CATHETER
Cardiovascular
27d
Cleared
Aug 08, 2012
CONVEY GUIDING CATHETER
Cardiovascular
163d