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

    MEDICAM 900 AUTOELECTRONIC LIGHT SOURCE

    K Number: K922544 · Decision Aug 7, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    75
    Registration Numbers
    75
    Same Product Code
    44
    Applicant Total
    76
    Review Days
    70

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    Basic Information

    Device Name
    MEDICAM 900 AUTOELECTRONIC LIGHT SOURCE
    K Number
    K922544
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4580
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Kirschner Medical Corp.
    Date Received
    May 29, 1992
    Decision Date
    August 7, 1992
    Product Code
    FST
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FST Light, Surgical, Fiberoptic

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