Device, Removal, Pacemaker Electrode, Percutaneous

FDA product code MFA · Class 3 · 6 devices · 433 reports · 106 deaths reported · 0 devices named in recalls

• GlideLight Laser Sheath 500-303

  Spectranetics Corporation · Device, Removal, Pacemaker Electrode, Percutaneous
  63 deaths221 reports
• GlideLight Laser Sheath 500-302

  Spectranetics Corporation · Device, Removal, Pacemaker Electrode, Percutaneous
  39 deaths180 reports
• GlideLight Laser Sheath 500-301

  Spectranetics Corporation · Device, Removal, Pacemaker Electrode, Percutaneous
  3 deaths27 reports
• SLS II Laser Sheath 500-001

  Spectranetics Corporation · Device, Removal, Pacemaker Electrode, Percutaneous
  2 reports
• SLS II Laser Sheath 500-013

  Spectranetics Corporation · Device, Removal, Pacemaker Electrode, Percutaneous
  1 death2 reports
• SLS II Laser Sheath 500-012

  Spectranetics Corporation · Device, Removal, Pacemaker Electrode, Percutaneous
  1 report