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

    ACCU PATH STERILE LABEL

    K Number: K904598 · Decision Oct 30, 1990
    View on FDA
    Classifications
    0
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    80
    Applicant Total
    1
    Review Days
    20

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    Basic Information

    Device Name
    ACCU PATH STERILE LABEL
    K Number
    K904598
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Accu-Path
    Date Received
    October 10, 1990
    Decision Date
    October 30, 1990
    Product Code
    LDQ
    Advisory Committee
    General Hospital
    Review Advisory Committee
    SU
    Third Party
    N

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