Medical Device Manufacturer · US , Danvers , MA

Medtronics Interventional Vascular - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1992

21

Total

21

Cleared

0

Denied

FDA 510(k) Regulatory Record - Medtronics Interventional Vascular Cardiovascular ✕

21 devices

1-12 of 21

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