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    ARTISAN MEDICAL

    FDA registration
    ARTISAN MEDICAL·18 products·🇺🇸 United States

    HANSEN MEDICAL ARTISAN S CONTROL CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HANSEN MEDICAL DILATOR FOR ARTISAN CONTROL CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SNAKE LIVER RETRACTOR 5MM

    FDA Adverse Event
    Malfunction ·ARTISAN MEDICAL·Product code GAD·October 11, 2018

    MARTIN ARM PAN

    FDA Adverse Event
    Malfunction ·ARTISAN MEDICAL·Product code GAD·May 7, 2025

    ARTISAN

    FDA Adverse Event
    Injury ·HANSEN MEDICAL, INC.·Product code DXX·September 25, 2012

    ARTISAN

    FDA Adverse Event
    Injury ·Product code DRA·September 10, 2008

    ARTISAN EXTEND CONTROL CATHETER

    FDA Adverse Event
    Injury ·HANSEN MEDICAL·Product code DRA·January 13, 2016

    ARTISAN

    FDA Adverse Event
    Injury ·HANSEN MEDICAL, INC.·Product code DXX·August 17, 2012

    ARTISAN EXTEND CONTROL CATHETER

    FDA Adverse Event
    Injury ·HANSEN MEDICAL, INC.·Product code DRA·October 23, 2014

    PRECISION SPECTRA®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 23, 2013

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 19, 2017

    Artisan brand Extend Control Catheter; An Steerable Guide Catheter; Component of Sensei X Robotic Catheter System; Model Number: 07546; Distributed and Manufactured by Hansen Medical, Inc, Mountain View, CA

    FDA Recall
    Terminated ·Hansen Medical Inc·Product code DXX·October 19, 2009

    PRECISION SPECTRA®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 11, 2014

    PRECISION SPECTRA®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 23, 2016

    ARTISAN EXTEND

    FDA Adverse Event
    Injury ·HANSEN MEDICAL, INC.·Product code DRA·August 6, 2015

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 27, 2014

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 5, 2012

    PRECISION SPECTRA

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 13, 2018

    PRECISION SPECTRA

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 19, 2018