Varian Medical Systems Inc

  • Manufacturer Address
    Varian Medical Systems Inc, 911 Hansen Way, Palo Alto CA 94303
  • Source
    USFDA
  • 1 Event

One device in the database

  • Model / Serial
    Affected Serial Numbers: 44, 260, 315, 495, 746, 751, 873, 907, 984, 1098, 1131, and 9045
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Product was released for distribution to 7 hospitals in the US. Distribution was limited to the following States: CA, MA, NC, SC, PA, and LA. 1 (one) Canadian distribution includes Fraser Valley Cancer Center, Dept. of Radiation Oncology, 13750 96th Ave., Surrey, BC, V3V 1Z2, Canada. Foreign distribution includes Austria, Germany and Finland. The recall was appropriately extended to the user level; i.e., the hospitals/physicians who received the recalled product.
  • Product Description
    VARiS 1.4G and Vision/SomaVision Radiation Therapy Systems; VARiS versions 6.1.33 and 6.2.19 in conjunction with Eclipse 6.x/Soma Vision 6.x

27 manufacturers with a similar name

Learn more about the data here

  • Manufacturer Address
    Varian Medical Systems Inc, 501 Locust Ave, Charlottesville VA 22902-4869
  • Manufacturer Parent Company (2017)
  • Source
    USFDA
  • Manufacturer Address
    Varian Medical Systems Inc, 3100 Hansen Way, Palo Alto CA 94304-1028
  • Source
    USFDA
  • Manufacturer Address
    Varian Medical Systems Inc, 3100 Hansen Way, M/S E-210, Palo Alto CA 94304-1030
  • Source
    USFDA
  • Manufacturer Address
    Varian Medical Systems Inc, 3100 Hansen Way, M/S E-210, Palo Alto CA 94304
  • Source
    USFDA
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