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

    URIN. L7-OH CORTICOSTEROID T(NON HYDRO)

    K Number: K761271 · Decision Feb 14, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    1
    Applicant Total
    4
    Review Days
    56

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    Basic Information

    Device Name
    URIN. L7-OH CORTICOSTEROID T(NON HYDRO)
    K Number
    K761271
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.1385
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Eppendorf-Brinkmann, Inc.
    Date Received
    December 20, 1976
    Decision Date
    February 14, 1977
    Product Code
    CDB
    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
    CDB Porter Silber Hydrazone, 17-Hydroxycorticosteroids

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (CDB), ordered by most recent decision date.

    17-HYDROXY TEST

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry
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    Other Clearances by Eppendorf-Brinkmann, Inc.

    K Number Device Name
    K780819 GLYCOHEMOGLOBIN-SKREEN TEST KIT
    K772337 URINARY 17-KETOSTERIOD/17
    K772151 URINARY VMA - SCREEN TEST KIT