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

    ATLAS ORTHOGONAL PERCUSSION INSTTUMENT

    K Number: K951217 · Decision Nov 21, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    13
    Registration Numbers
    13
    Same Product Code
    31
    Applicant Total
    1
    Review Days
    249

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    Basic Information

    Device Name
    ATLAS ORTHOGONAL PERCUSSION INSTTUMENT
    K Number
    K951217
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Sweat Chiropractic Clinic
    Date Received
    March 17, 1995
    Decision Date
    November 21, 1995
    Product Code
    LXM
    Advisory Committee
    Unknown
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LXM Manipulator, Plunger-Like Joint

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