Device, Angioplasty, Laser, Coronary
FDA product code LPC · Class 3 · 9 devices · 56 reports · 3 deaths reported · 1 devices named in recalls
- Philips Laser System LAS-100Spectranetics Corporation · Device, Angioplasty, Laser, Coronary2 recalls9 reports
- ELCA Coronary Laser Atherectomy Catheter 110-004Spectranetics Corporation · Device, Angioplasty, Laser, Coronary2 deaths31 reports
- ELCA Coronary Laser Atherectomy Catheter 114-009Spectranetics Corporation · Device, Angioplasty, Laser, Coronary7 reports
- ELCA Coronary Laser Atherectomy Catheter 117-016Spectranetics Corporation · Device, Angioplasty, Laser, Coronary3 reports
- ELCA™ 110-004AASpectranetics Corporation · Device, Angioplasty, Laser, Coronary2 reports
- ELCA™ 114-009AASpectranetics Corporation · Device, Angioplasty, Laser, Coronary1 report
- ELCA™ 117-016AASpectranetics Corporation · Device, Angioplasty, Laser, Coronary1 report
- ELCA™ 117-205ABSpectranetics Corporation · Device, Angioplasty, Laser, Coronary1 report
- ELCA Coronary Laser Atherectomy Catheter 110-002Spectranetics Corporation · Device, Angioplasty, Laser, Coronary1 death1 report