BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    HIGH PRESSURE FLEX. CONNECTING TUBING

    K Number: K841092 · Decision Jul 24, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    124
    Registration Numbers
    124
    Same Product Code
    209
    Applicant Total
    12
    Review Days
    498

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    Basic Information

    Device Name
    HIGH PRESSURE FLEX. CONNECTING TUBING
    K Number
    K841092
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1650
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Tronomed, Inc.
    Date Received
    March 13, 1984
    Decision Date
    July 24, 1985
    Product Code
    DXT
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    DXT Injector And Syringe, Angiographic

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    Other Clearances by Tronomed, Inc.

    K Number Device Name
    K952659 TRONOMATE PATIENT CABLE & LEADWIRE SYSTEM
    K853303 LIFELINC LEADWIRE
    K853452 LIFE LINC PATIENT CABLE
    K792125 3&4 WAY PLASTIC STOPCOCKS, NONSTERILE
    K792128 STERILE EXTENSION TUBES INDIV. PKG.
    K792124 TANDEM ASSEMBLED 3&4 WAY STOPCOCKS
    K792126 3&4 WAY PLASTIC STERILE STPCKS. PKG.
    K792127 PLAS. STCK. W/EXTENSION TUBE/STERILE
    K771645 ELECTROCARDIOGRAPHIC CABLHS & LEAD WIRE
    K771027 ELECTROCARDIOGRAPHIC PATIENT CABLES
    Search all 12 clearances from Tronomed, Inc. →