Medtronic Cryocath, LP - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Medtronic Cryocath, LP has 6 FDA 510(k) cleared medical devices. Based in Kirkland, CA.
Historical record: 6 cleared submissions from 2010 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medtronic Cryocath, LP Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Medtronic Cryocath, LP
6 devices
Cleared
Nov 13, 2020
FlexCath Advance Steerable Sheath and Dilator
Cardiovascular
64d
Cleared
Nov 26, 2018
FlexCath Advance Steerable Sheath and Dilator
Cardiovascular
10d
Cleared
Feb 02, 2017
FlexCath Select Steerable Shealth and Dilator
Cardiovascular
73d
Cleared
Nov 06, 2014
FlexCath Select Steerable Sheath (10 French)
Cardiovascular
48d
Cleared
Dec 27, 2012
FLEXCATH ADVANCE STEERABLE SHEATH (12 FRENCH)
Cardiovascular
36d
Cleared
Sep 01, 2010
FLEXCATH STEERABLE SHEATH (12 FRENCH), FLEXCATH STEERABLE SHEATH (10 FRENCH)...
Cardiovascular
29d