Device Recall LIGHTWAVE SUCTION ABLATOR

  • Modèle / numéro de série
    All lots manufactured from July 2004 to September 2008: Lot Numbers: 0407121, 0407151, 0407211, 0407271, 0411151, 0411221, 0411291, 0412081, 0412111, 0502161, 0502211, 0504281, 0505021, 0505061, 0505091, 0505101, 0505121, 0505161, 0505171, 0505231, 0506021, 0506131, 0507051, 0508121, 0508221, 0508251, 0509061, 0511021, 0511091, 0511301, 0602231, 0604241, 0606071, 0606191, 0610271, 0611011, 0703121, 0703191, 0704021, 0704091, 0704121, 0705091, 0705231, 0706041, 0706221, 0706271, 0707241, 0708031, 0708131, 0708201, 0711261, 0711301, 0801072, 0801152, 0802132, 0802202, 0803072, 0803112, 0803262, 0803312, 0804171, 0804292, 0805022, 0805061, 0805062, 0806092, 0806262, 0807142, 0807232, 0807292, 0808052, 0808132, 0809032, 0809052, and 0809262.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution
  • Description du dispositif
    REF IA-2000-S, LightWave Suction Ablator, STERILE, Rx ONLY, MADE IN USA. || CONMED LINVATEC, 11311 CONCEPT BLVD, LARGO, FL 33773-4908. || ConMed Linvatec LIGHTWAVE SUCTION ABLATOR, electrosurgical cutting and coagulation device and accessories, intended to remove tissue and control bleeding by use of high-frequency electrical current.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Linvatec Corp. dba ConMed Linvatec, 11311 Concept Blvd, Largo FL 33773-4908
  • Société-mère du fabricant (2017)
  • Source
    USFDA