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

    RIGHT TIME RHYTHM CLOCK

    K Number: K823463 · Decision Mar 17, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    28
    Registration Numbers
    28
    Same Product Code
    23
    Applicant Total
    2
    Review Days
    118

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    Basic Information

    Device Name
    RIGHT TIME RHYTHM CLOCK
    K Number
    K823463
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Applicant
    P.K. Morgan Instruments, Inc.
    Date Received
    November 19, 1982
    Decision Date
    March 17, 1983
    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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    Other Clearances by P.K. Morgan Instruments, Inc.

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