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

    NEONATAL BLOOD SPOT TEST 17-HYDROXPROG RADIO KIT

    K Number: K911839 · Decision Jun 18, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    22
    Registration Numbers
    22
    Same Product Code
    18
    Applicant Total
    16
    Review Days
    54

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    Basic Information

    Device Name
    NEONATAL BLOOD SPOT TEST 17-HYDROXPROG RADIO KIT
    K Number
    K911839
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.1395
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Pantex, Div. Bio-Analysis, Inc.
    Date Received
    April 25, 1991
    Decision Date
    June 18, 1991
    Product Code
    JLX
    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
    JLX Radioimmunoassay, 17-Hydroxyprogesterone

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