Catheter, intravascular, diagnostic
FDA product code DQO · Class 2 · 810 devices · 2,516 reports · 21 deaths reported · 253 devices named in recalls
- Soft-Vu 50702301Angiodynamics, Inc. · CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- Soft-Vu 50722631Angiodynamics, Inc. · CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- NAMIC 88001483Navilyst Medical, Inc. · CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- NAMIC 90703050Navilyst Medical, Inc. · CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- NAMIC 90703122Navilyst Medical, Inc. · CATHETER, INTRAVASCULAR, DIAGNOSTIC1 report
- Twin-Pass® 023" dual access catheter 5230Vascular Solutions, Inc. · Catheter, Intravascular, Diagnostic1 report
- Langston® dual lumen catheter 5515Vascular Solutions, Inc. · Catheter, Intravascular, Diagnostic1 report
- Langston® dual lumen catheter 5550Vascular Solutions, Inc. · Catheter, Intravascular, Diagnostic1 report
- GrebSet® micro-introducer kit 7941Vascular Solutions, Inc. · Catheter, Intravascular, Diagnostic1 report
- GrebSet® micro-introducer kit 7951Vascular Solutions, Inc. · Catheter, Intravascular, Diagnostic1 report