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

    FERTILITY FORECASTER COMPUTER PROGRAM

    K Number: K880618 · Decision Jun 24, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    28
    Registration Numbers
    28
    Same Product Code
    23
    Applicant Total
    1
    Review Days
    129

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    Basic Information

    Device Name
    FERTILITY FORECASTER COMPUTER PROGRAM
    K Number
    K880618
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Applicant
    Fertile Time, Ltd.
    Date Received
    February 16, 1988
    Decision Date
    June 24, 1988
    Product Code
    LHD
    Advisory Committee
    Unknown
    Review Advisory Committee
    OB
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LHD Device, Fertility Diagnostic, Proceptive

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