Devices

Device Recall Rita Thermopads

  • Modelo / Serial
    Lot codes affected: Y110503-1 and Y103003-2. 510k number : k031926 Contract manufacturer, Katecho, Inc, registration number 1932007
  • Clasificación del producto
    General and Plastic Surgery Devices
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Product was shipped to 18 field representatives and 87 customers (hospitals and medical centers
  • Descripción del producto
    Dispersive Electrodes packaged in an 8x10 plastic container.
  • Manufacturer
    Rita Medical Systems
  • 1 Event

Fabricante

Rita Medical Systems
  • Dirección del fabricante
    Rita Medical Systems, 967 N Shoreline Blvd, Mountain View CA 94043-1932
  • Source
    USFDA