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

    POINT LOCATOR STIMULATOR

    K Number: K792529 · Decision Feb 26, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    2
    Applicant Total
    14
    Review Days
    81

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    Basic Information

    Device Name
    POINT LOCATOR STIMULATOR
    K Number
    K792529
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5580
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Staodynamics, Inc.
    Date Received
    December 7, 1979
    Decision Date
    February 26, 1980
    Product Code
    BWJ
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    BWJ Locator, Acupuncture Point

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