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

    MRS-2D

    K Number: K961645 · Decision Oct 31, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    101
    Registration Numbers
    101
    Same Product Code
    171
    Applicant Total
    3
    Review Days
    185

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    Basic Information

    Device Name
    MRS-2D
    K Number
    K961645
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.5050
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Lexicor Medical Technology, Inc.
    Date Received
    April 29, 1996
    Decision Date
    October 31, 1996
    Product Code
    HCC
    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
    HCC Device, Biofeedback

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    Other Clearances by Lexicor Medical Technology, Inc.

    K Number Device Name
    K915820 NEUROSEARCH-24 OR NRS-24
    K904269 NEUROSEARCH-24 OR NRS-24