Devices

Device Recall Laser Guide Catheter

  • Model / Serial
    Lot Numbers: CTB09K14A, FTB09L25C, FTB09M01A, FTB09M02A, FTB10B10B, FTB10F28A, FTB10G12A.
  • Product Classification
    Cardiovascular Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Foreign Distribution-including the countries of Belgium, Cyprus, Germany, Greece, Italy, Spain, Switzerland, and United Kingdom.
  • Product Description
    Spectranetics Turbo-Booster Laser Guide Catheter, 7 Fr, REF 518-043, Sterile EO, Spectranetics Corporation, 96 Talamine Court, Colorado Springs, CO 80907. || Designed for directing and supporting Spectranetics laser catheters for use in the treatment of infrainguinal stenoses and occlusions.
  • Manufacturer
    Spectranetics Corporation
  • 1 Event

Manufacturer

Spectranetics Corporation
  • Manufacturer Address
    Spectranetics Corporation, 96 Talamine Ct, Colorado Springs CO 80907-5159
  • Manufacturer Parent Company (2017)
    Philips
  • Source
    USFDA

One device with a similar name

Learn more about the data here

Device Recall Laser Guide Catheter
  • Model / Serial
    Lot Numbers: CMP09L24C, CTB09G21A, FTB09M11A, FTB10C02A, FTB10F14A, FTB10H17B, FTB11D12A.
  • Product Classification
    Cardiovascular Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Foreign Distribution-including the countries of Belgium, Cyprus, Germany, Greece, Italy, Spain, Switzerland, and United Kingdom.
  • Product Description
    Spectranetics Turbo-Booster Laser Guide Catheter, 8 Fr, REF 518-063, Sterile EO, Spectranetics Corporation, 96 Talamine Court, Colorado Springs, CO 80907. || Designed for directing and supporting Spectranetics laser catheters for use in the treatment of infrainguinal stenoses and occlusions.
  • Manufacturer
    Spectranetics Corporation