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    M2376A DEVICELINK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFICATION TO M2376A DEVICELINK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INTELLIVUE PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PHILIPS MP40, MP50, MP60, MP70, MP80 AND MP90 INTELLIVUE PATIENT MONITORS, RELEASE D.00

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VENUS Bracket, ROSE Bracket

    FDA 510(k)
    FDA Class 2 ·Dental

    THE PHILLIPS, MODEL MP20,MP30,MP40,MP50,MP60,MP70,MP80,AND MP90 INTELLIVUE PATIENT MONITORS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    THE PHILIPS MP20,MP30,MP40,MP50,MP60,MP70,MP80 AND MP90 INTELLIVUE ATIENT MONITORS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    M2376A PHILIPS DEVICE LINK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SLIMUS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MODIFICATION TO AGILENT TECHNOLOGIES ANESTHESIA GAS MONITOR, MODEL M1026A #CO5

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    INTELLIVUE PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    HP ORVUE INTRA-OP (M2510A)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    INTELLIVUE PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    INTELLIVUE PATIENT MONITOR, INTELLIBRIDGE MODULE, MODELS MP40, MP50, MP60, MP70, MP80, MP90, EC10, EC5

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Zavation

    FDA UDI
    ZAVATION LLC·00197157005771·8G 20mm Bipedicular Kit Additional

    Zavation

    FDA UDI
    ZAVATION LLC·00197157005757·8G 10mm Bipedicular Kit Additional

    Zavation

    FDA UDI
    ZAVATION LLC·00197157005764·8G 15mm Bipedicular Kit Additional

    Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

    FDA Pre-Market Approval
    FDA Class 3 ·COROX OTW (-S) BP STEROID-ELUTING LEADS

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·SELOX SR/ST/JT, SETROX S, AND DEXTRUS STEROID-ELUTING LEADS

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·KENTROX SL/SL-S/RV/RV-S & LINOX S/SD/T/TD STEROID-ELUTING LEADS