Device Recall Flexor CheckFlo Introducer

  • Modèle / numéro de série
    Catalog #:  KCFW-6.0-35-70-RB-HFANL0-HC  Lot: 6166304
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed in the states of CA, FL, OK, OH, MI, TX, NJ, and NY.
  • Description du dispositif
    Flexor Check-Flo Introducer, Catheter introducer, || Catalog #: KCFW-6.0-35-70-RB-HFANL0-HC || Intended for introduction of balloons, closed and non-tapered end catheters or diagnostic and interventional devices
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Cook Inc., 750 N Daniels Way, Bloomington IN 47404-9120
  • Société-mère du fabricant (2017)
  • Source
    USFDA