Drug-Eluting Peripheral Transluminal Angioplasty Catheter
FDA product code ONU · Class 3 · 207 devices · 1,733 reports · 11 deaths reported · 17 devices named in recalls
- SurVeil DCB SRV03513504015Surmodics, Inc. · Drug-Eluting Peripheral Transluminal Angioplasty Catheter1 report
- Stellarex AB35SX050120135Spectranetics Corporation · Drug-Eluting Peripheral Transluminal Angioplasty Catheter1 report
- Stellarex AB35SX040200135Spectranetics Corporation · Drug-Eluting Peripheral Transluminal Angioplasty Catheter1 report
- Stellarex AB35SX050200135Spectranetics Corporation · Drug-Eluting Peripheral Transluminal Angioplasty Catheter1 report
- Stellarex AB35SX060120135Philips Image Guided Therapy Corporation · Drug-Eluting Peripheral Transluminal Angioplasty Catheter1 report
- Stellarex AB35SX060200135Philips Image Guided Therapy Corporation · Drug-Eluting Peripheral Transluminal Angioplasty Catheter1 report
- Ranger™ H74939419702010Boston Scientific Corporation · Drug-Eluting Peripheral Transluminal Angioplasty Catheter1 report