Invatec Innovative Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Invatec Innovative Technologies - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Invatec Innovative Technologies has 3 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 3 cleared submissions from 2004 to 2006. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Invatec Innovative Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Invatec Innovative Technologies
3 devices
Cleared
Oct 18, 2006
ADMIRAL XTREME PTA CATHETER
Cardiovascular
29d
Cleared
Nov 08, 2004
SUBMARINE PLUS PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER, MODEL...
Cardiovascular
49d
Cleared
Nov 08, 2004
SAILOR PLUS PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) CATHETER, MODEL...
Cardiovascular
49d