Device, Biopsy, Endomyocardial

FDA product code DWZ · Class 2 · 14 devices · 25 reports · 0 devices named in recalls

• Cook G05389

  Cook Incorporated · DEVICE, BIOPSY, ENDOMYOCARDIAL
  3 reports
• Jawz Endomyocardial Biopsy Forceps 190075

  Argon Medical Devices, Inc. · Device, Biopsy, Endomyocardial
  3 reports
• Biopsy Forceps 504300

  Cordis US Corp. · DEVICE, BIOPSY, ENDOMYOCARDIAL
  3 reports
• Jawz Endomyocardial Biopsy Forceps 190030

  Argon Medical Devices, Inc. · Device, Biopsy, Endomyocardial
  2 reports
• Jawz Endomyocardial Biopsy Forceps 190051

  Argon Medical Devices, Inc. · Device, Biopsy, Endomyocardial
  2 reports
• Jawz Endomyocardial Biopsy Forceps 190070

  Argon Medical Devices, Inc. · Device, Biopsy, Endomyocardial
  2 reports
• Jawz Endomyocardial Biopsy Forceps 190081

  Argon Medical Devices, Inc. · Device, Biopsy, Endomyocardial
  2 reports
• Biopsy Forceps 504302

  Cordis Corporation · DEVICE, BIOPSY, ENDOMYOCARDIAL
  2 reports
• Cook G05533

  Cook Incorporated · DEVICE, BIOPSY, ENDOMYOCARDIAL
  1 report
• Jawz Endomyocardial Biopsy Forcep 190065

  Argon Medical Devices, Inc. · Device, Biopsy, Endomyocardial
  1 report
• Jawz Endomyocardial Biopsy Forceps 190085

  Argon Medical Devices, Inc. · Device, Biopsy, Endomyocardial
  1 report
• Jawz Endomyocardial Biopsy Forcep 190095

  Argon Medical Devices, Inc. · Device, Biopsy, Endomyocardial
  1 report
• Procure™ 408296

  St. Jude Medical, Inc. · DEVICE, BIOPSY, ENDOMYOCARDIAL
  1 report
• Procure™ 408298

  St. Jude Medical, Inc. · DEVICE, BIOPSY, ENDOMYOCARDIAL
  1 report