Devices

Device Recall Desktop Pro Linear Medical Accelerator

  • Modèle / numéro de série
    Model number MRT 9871/ MRT 10601 (This issue affects Desktop Pro 6.0 and 6.1 users with a 3rd party R & V System, with the exception of Sigma Micro Users)
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide distribution ---- including USA states of AZ, AL, CA, CO, FL, GA, IA, MI, NV, OH, OK, PA, WA, WV and Country of Canada .
  • Description du dispositif
    Desktop Pro¿ R6.0 & R6.1, Linear Medical Accelerator.
  • Manufacturer
    Elekta, Inc.
  • 1 Event

Fabricant

Elekta, Inc.
  • Adresse du fabricant
    Elekta, Inc., 4775 Peachtree Industrial Blvd., Building 300, Suite 300, Norcross GA 30092-3023
  • Source
    USFDA