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

    VACU-PREP

    K Number: K864923 · Decision Jan 20, 1987
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    35

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    Basic Information

    Device Name
    VACU-PREP
    K Number
    K864923
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Diversified High Tech Co.
    Date Received
    December 16, 1986
    Decision Date
    January 20, 1987
    Advisory Committee
    Unknown
    Review Advisory Committee
    SU
    Third Party
    N