Devices

Device Recall Philips Allura Xper FD20

  • Model / Serial
    2786
  • Product Classification
    Radiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    US: WA OUS: China, Spain, Korea, Republic of, Germany
  • Product Description
    Allura Xper FD20 722012 is intended for: Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and atherectomies), pacemaker implantations and Electro Physiology(EP).
  • Manufacturer
    Philips Electronics North America Corporation
  • 1 Event

Manufacturer

Philips Electronics North America Corporation
  • Manufacturer Address
    Philips Electronics North America Corporation, 3000 Minuteman Rd, Andover MA 01810-1032
  • Manufacturer Parent Company (2017)
    Philips
  • Source
    USFDA

One device with a similar name

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Device Recall Philips Allura Xper FD20 R8.2 722028
  • Model / Serial
    1000
  • Product Classification
    Radiology Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    US: WA OUS: China, Spain, Korea, Republic of, Germany
  • Product Description
    Allura Xper FD20 R8.2 722028 is intended for: Cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and atherectomies), pacemaker implantations and Electrophysiology(EP).
  • Manufacturer
    Philips Electronics North America Corporation