BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    EURO TECH DIAMOND CHIROPRACTIC TABLE

    K Number: K943972 · Decision Oct 11, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    51
    Registration Numbers
    51
    Same Product Code
    101
    Applicant Total
    10
    Review Days
    57

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    Basic Information

    Device Name
    EURO TECH DIAMOND CHIROPRACTIC TABLE
    K Number
    K943972
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    890.3760
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Progressive Electrical Therapeutics
    Date Received
    August 15, 1994
    Decision Date
    October 11, 1994
    Product Code
    INQ
    Advisory Committee
    Physical Medicine
    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
    INQ Table, Powered

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