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

    ENDOPATH ENDO-SURGERY PERCUTANEOUS CATHETER INTROD

    K Number: K921833 · Decision Sep 21, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    548
    Registration Numbers
    548
    Same Product Code
    747
    Applicant Total
    204
    Review Days
    158

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    Basic Information

    Device Name
    ENDOPATH ENDO-SURGERY PERCUTANEOUS CATHETER INTROD
    K Number
    K921833
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5860
    Medical Specialty
    General Hospital
    Decision
    Unknown
    Statement or Summary
    Summary
    Applicant
    ETHICON, Inc.
    Date Received
    April 16, 1992
    Decision Date
    September 21, 1992
    Product Code
    FMF
    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
    FMF Syringe, Piston

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