BEUDAMED
    FDA 510(k) Unknown 🇺🇸 United States

    OCCUPAK CAT.#200-0538

    K Number: K802691 · Decision Oct 27, 1980
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    2
    Review Days
    —

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    Basic Information

    Device Name
    OCCUPAK CAT.#200-0538
    K Number
    K802691
    Clearance Type
    Traditional
    Decision
    Unknown
    Applicant
    Occumedics, Inc.
    Date Received
    October 27, 1980
    Decision Date
    October 27, 1980
    Advisory Committee
    Unknown
    Review Advisory Committee
    OP
    Third Party
    N

    Other Clearances by Occumedics, Inc.

    K Number Device Name
    K802690 ULTRAPAK CAT. #100-0251