Port & catheter, implanted, subcutaneous, intraventricular

FDA product code LKG · Class 2 · 10 devices · 50 reports · 0 devices named in recalls

• N/A 44010

  Medtronic Ps Medical, Inc. · Port & catheter, implanted, subcutaneous, intraventricular
  30 reports
• NA 44010

  Medtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR
  9 reports
• NA 41406

  Medtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR
  2 reports
• NA 41407

  Medtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR
  2 reports
• N/A 41406

  Medtronic Ps Medical, Inc. · Port & catheter, implanted, subcutaneous, intraventricular
  2 reports
• NA 44102

  Medtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR
  1 report
• Innervision 27065 C

  Medtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR
  1 report
• Innervision 27065 B

  Medtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR
  1 report
• NA 27051

  Medtronic Ps Medical, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVENTRICULAR
  1 report
• N/A 41409

  Medtronic Ps Medical, Inc. · Port & catheter, implanted, subcutaneous, intraventricular
  1 report