Invatec S.P.A. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Invatec S.P.A. - FDA 510(k) Cleared Devices
4
Total
3
Cleared
0
Denied
Invatec S.P.A. has 3 FDA 510(k) cleared medical devices. Based in Bethlehem, US.
Historical record: 3 cleared submissions from 2009 to 2010. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Invatec S.P.A. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Invatec S.P.A.
4 devices
Cleared
Apr 30, 2010
ADMIRAL XTREME PTA BALLOON DILATATION CATHETER
Cardiovascular
28d
Cleared
Mar 16, 2010
SCUBA BILIARY STENT SYSTEM
Gastroenterology & Urology
224d
Cleared
Oct 29, 2009
REEF HP 0.035 OTW PTA BALLOON DILATATION CATHETER
Cardiovascular
86d
Cleared
Oct 15, 2009
MO.MA ULTRA PROXIMAL CEREBRAL PROTECTION DEVICE, MODEL MUS0130069X6
Cardiovascular
86d