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

    ACU-DOT

    K Number: K781672 · Decision Nov 8, 1978
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    36

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    Basic Information

    Device Name
    ACU-DOT
    K Number
    K781672
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Acu-Dot Pharmaceutical Intl., Inc.
    Date Received
    October 3, 1978
    Decision Date
    November 8, 1978
    Advisory Committee
    Unknown
    Review Advisory Committee
    SU
    Third Party
    N