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

    MPC-150 MALE TO MALE LUER ADAPTER

    K Number: K925930 · Decision Aug 16, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    424
    Registration Numbers
    424
    Same Product Code
    1173
    Applicant Total
    7
    Review Days
    266

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    Basic Information

    Device Name
    MPC-150 MALE TO MALE LUER ADAPTER
    K Number
    K925930
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5440
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Molded Products, Inc.
    Date Received
    November 23, 1992
    Decision Date
    August 16, 1993
    Product Code
    FPA
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FPA Set, Administration, Intravascular

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    Other Clearances by Molded Products, Inc.

    K Number Device Name
    K022068 TUBING, DIALYSATE (AND CONNECTOR)
    K010366 DISPOSABLE STORAGE CAP
    K010712 DIALYSATE LINE WITH CONNECTORS/RE-USE WASH-OUT LINES
    K003712 MODIFICATION TO MALE TO MALE LUER ADAPTER
    K925978 MPC-80 TRANSDUCER
    K925927 MPC-1000 INJECTION CAP/PLUG