Medtronics Interventional Vascular is one of 5565 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medtronics Interventional Vascular - FDA 510(k) Cleared Devices
Recent clearances: MEDTRONIC 5F & 9F ZUMA GUIDING CATHETERS, MEDTRONIC ANGIOGRAPHIC CATHETER, MEDTRONIC 7F AND 8F ZUMA GUIDING CATHETER
21
Total
21
Cleared
0
Denied
Medtronics Interventional Vascular has 21 FDA 510(k) cleared cardiovascular devices. Based in Danvers, US.
Historical record: 21 cleared submissions from 1992 to 1999.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medtronics Interventional Vascular
21 devices
Cleared
Mar 22, 1999
MEDTRONIC 5F & 9F ZUMA GUIDING CATHETERS
Cardiovascular
18d
Cleared
Dec 10, 1998
MEDTRONIC ANGIOGRAPHIC CATHETER
Cardiovascular
269d
Cleared
Sep 04, 1998
MEDTRONIC 7F AND 8F ZUMA GUIDING CATHETER
Cardiovascular
18d
Cleared
Aug 07, 1998
MEDTRONIC ZUMA GUIDING CATHETER
Cardiovascular
127d
Cleared
Nov 03, 1997
MEDTRONIC MUSTANG SUPER FLOPPY GUIDE WIRE/FLOPPY GUIDE WIRE/INTERMEDIATE...
Cardiovascular
84d
Cleared
Nov 20, 1996
MEDTRONIC MUSTANG STEERABLE GUIDE WIRE (M-45FR, M45FX)
Cardiovascular
187d
Cleared
May 30, 1996
MEDTRONIC EVERST 30 INFLATION DEVICE/SURVIVAL KIT
Cardiovascular
80d
Cleared
Jan 22, 1996
MEDTRONIC SHERPA GUIDING CATHETER
Cardiovascular
41d
Cleared
Nov 21, 1995
MEDTRONIC GC IV CORONARY GUIDING CATHETER
Cardiovascular
288d
Cleared
Jul 25, 1995
MEDTRONIC(R) GC III CORONARY GUIDING CATHETER
Cardiovascular
189d
Cleared
Apr 05, 1995
MEDTRONIC(R) 8.2 FRENCH SHERPA(R) SUPER PEAK FLOW(TM) CORONARY GUIDING CATHETER
Cardiovascular
91d
Cleared
Mar 03, 1995
SHERPA SHERPA II AND ASCENT CORONARY GUIDING CATHETERS
Cardiovascular
171d