Device Recall Dr. Fog

  • Model / Serial
    Lot 2007-05-25; exp. May 2007.
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide.
  • Product Description
    Dr. Fog Endoscopic fog prevention kit.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Aspen Surgical Products, Inc., 7425 Clyde Park Ave Sw Ste G, Byron Center MI 49315-8373
  • Source
    USFDA