BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    NEONATAL BIOTINIDASE KIT, MODEL 3018

    K Number: K090123 · Decision Mar 5, 2010
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2
    Same Product Code
    4
    Applicant Total
    17
    Review Days
    408

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    Basic Information

    Device Name
    NEONATAL BIOTINIDASE KIT, MODEL 3018
    K Number
    K090123
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1118
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Perkinelmer, Inc.
    Date Received
    January 21, 2009
    Decision Date
    March 5, 2010
    Product Code
    NAK
    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
    NAK System, Test, Biotinidase

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