Cordis US Corp - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Cordis US Corp has 4 FDA 510(k) cleared medical devices. Based in Miami Lakes, US.
Latest FDA clearance: Jun 2024. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Cordis US Corp Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Cordis US Corp
4 devices
Cleared
Jun 28, 2024
Cordis BRITECROSS Support Catheter
Cardiovascular
228d
Cleared
Nov 21, 2023
INFINITI™ Ambi Angiographic Catheter
Cardiovascular
88d
Cleared
Apr 24, 2023
RAIN Sheath™ Tibial Pedal Introducer
Cardiovascular
41d
Cleared
Aug 22, 2022
SABER .014 PTA Dilatation Catheter
Cardiovascular
60d