BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    JACKSON CROSS CYLINDER TEST

    K Number: K873915 · Decision Oct 28, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    0
    Applicant Total
    15
    Review Days
    33

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    Basic Information

    Device Name
    JACKSON CROSS CYLINDER TEST
    K Number
    K873915
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    886.1840
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Applicant
    Richmond Products, Inc.
    Date Received
    September 25, 1987
    Decision Date
    October 28, 1987
    Product Code
    HOR
    Advisory Committee
    Ophthalmic
    Review Advisory Committee
    OP
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HOR Simulatan (Including Crossed Cylinder)

    Other Clearances by Richmond Products, Inc.

    K Number Device Name
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    K874250 THREE CHAR. TEST-CHILD & WORTH 4 DOT TEST NEARPT.
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    K873907 CONFIRMATION TESTS
    K873908 H.R.R. PSEUDOISOCHROMATIC COLOR BLINDNESS TEST BK.
    K873916 'E' CUBE AND 'E' PAD
    K873914 ANIMATED FIXATION TOYS (DISTANCE AND NEARPOINT)
    K873913 COLOR BOOK ILLUMINATOR STAND
    K873911 PSEUDO ISOCHROMATIC COLOR BLINDNESS TEST BOOK - 15
    K873917 TONOMETER TAPES
    Search all 15 clearances from Richmond Products, Inc. →