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

    AUTONOM

    K Number: K780312 · Decision Apr 5, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    63
    Registration Numbers
    63
    Same Product Code
    1
    Applicant Total
    2
    Review Days
    49

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    Basic Information

    Device Name
    AUTONOM
    K Number
    K780312
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    890.5765
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    Autonomic Equipment Supply Co,
    Date Received
    February 15, 1978
    Decision Date
    April 5, 1978
    Product Code
    KNM
    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
    KNM Device, Pressure Applying

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (KNM), ordered by most recent decision date.

    AUTONORM & NERV-A-NORM

    FDA 510(k)
    FDA Class 1 ·Physical Medicine
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    Other Clearances by Autonomic Equipment Supply Co,

    K Number Device Name
    K811956 AUTONORM & NERV-A-NORM