Device Recall Rita Thermopads

  • Modèle / numéro de série
    Lot codes affected: Y110503-1 and Y103003-2. 510k number : k031926 Contract manufacturer, Katecho, Inc, registration number 1932007
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Product was shipped to 18 field representatives and 87 customers (hospitals and medical centers
  • Description du dispositif
    Dispersive Electrodes packaged in an 8x10 plastic container.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Rita Medical Systems, 967 N Shoreline Blvd, Mountain View CA 94043-1932
  • Source
    USFDA