Medical Device Manufacturer · US , Danvers , MA

Medtronics Interventional Vascular - FDA 510(k) Cleared Devices

21 submissions · 21 cleared · Since 1992

Total

Cleared

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

1-12 of 21

Cleared Mar 22, 1999

MEDTRONIC 5F & 9F ZUMA GUIDING CATHETERS

K990707 · DQY

Cardiovascular · 18d

Cleared Dec 10, 1998

MEDTRONIC ANGIOGRAPHIC CATHETER

K980973 · DQO

Cardiovascular · 269d

Cleared Sep 04, 1998

MEDTRONIC 7F AND 8F ZUMA GUIDING CATHETER

K982883 · DQY

Cardiovascular · 18d

Cleared Aug 07, 1998

MEDTRONIC ZUMA GUIDING CATHETER

K981198 · DQY

Cardiovascular · 127d

Cleared Nov 03, 1997

MEDTRONIC MUSTANG SUPER FLOPPY GUIDE WIRE/FLOPPY GUIDE WIRE/INTERMEDIATE...

K972944 · DQX

Cardiovascular · 84d

Cleared Nov 20, 1996

MEDTRONIC MUSTANG STEERABLE GUIDE WIRE (M-45FR, M45FX)

K961917 · DQX

Cardiovascular · 187d

Cleared May 30, 1996

MEDTRONIC EVERST 30 INFLATION DEVICE/SURVIVAL KIT

K960983 · MAV

Cardiovascular · 80d

Cleared Jan 22, 1996

MEDTRONIC SHERPA GUIDING CATHETER

K955651 · DQY

Cardiovascular · 41d

Cleared Nov 21, 1995

MEDTRONIC GC IV CORONARY GUIDING CATHETER

K950490 · DQY

Cardiovascular · 288d

Cleared Jul 25, 1995

MEDTRONIC(R) GC III CORONARY GUIDING CATHETER

K950179 · DQY

Cardiovascular · 189d

Cleared Apr 05, 1995

MEDTRONIC(R) 8.2 FRENCH SHERPA(R) SUPER PEAK FLOW(TM) CORONARY GUIDING CATHETER

K950026 · DQY

Cardiovascular · 91d

Cleared Mar 03, 1995

SHERPA SHERPA II AND ASCENT CORONARY GUIDING CATHETERS

K944668 · DQY

Cardiovascular · 171d

Medtronics Interventional Vascular - FDA 510(k) Cleared Devices

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