BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

    Background Pattern Classification [BPc(TM)]

    K Number: K152301 · Decision Jun 3, 2016
    View on FDA
    Classifications
    1
    FEI Numbers
    13
    Registration Numbers
    13
    Same Product Code
    15
    Applicant Total
    12
    Review Days
    294

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    Basic Information

    Device Name
    Background Pattern Classification [BPc(TM)]
    K Number
    K152301
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.1400
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Natus Medical Incorporated Dba Excel-Tech Ltd. (Xltek)
    Date Received
    August 14, 2015
    Decision Date
    June 3, 2016
    Product Code
    OMA
    Advisory Committee
    Neurology
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    OMA Amplitude-Integrated Electroencephalograph

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