Cordis US Corp - FDA 510(k) Cleared Devices
Recent clearances: Cordis BRITECROSS Support Catheter, INFINITI™ Ambi Angiographic Catheter, RAIN Sheath™ Tibial Pedal Introducer
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cordis US Corp Cardiovascular ✕
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