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

    LB 9502 - CLINILUMAT, LB 952 - AUTO-CLINILUMAT

    K Number: K872324 · Decision Aug 19, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    85
    Registration Numbers
    85
    Same Product Code
    257
    Applicant Total
    2
    Review Days
    63

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    Basic Information

    Device Name
    LB 9502 - CLINILUMAT, LB 952 - AUTO-CLINILUMAT
    K Number
    K872324
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.2300
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Berthold Analytical Instruments, Inc.
    Date Received
    June 17, 1987
    Decision Date
    August 19, 1987
    Product Code
    JJQ
    Advisory Committee
    Clinical Chemistry
    Review Advisory Committee
    CH
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use

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