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

    700 SERIES BIOMAGNETOMETER

    K Number: K901215 · Decision Jun 25, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    12
    Registration Numbers
    12
    Same Product Code
    23
    Applicant Total
    8
    Review Days
    103

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    Basic Information

    Device Name
    700 SERIES BIOMAGNETOMETER
    K Number
    K901215
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.1400
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Applicant
    Biomagnetic Technologies, Inc.
    Date Received
    March 14, 1990
    Decision Date
    June 25, 1990
    Product Code
    OLX
    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
    OLX Source Localization Software For Electroencephalograph Or Magnetoencephalograph

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