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

    PNEUMATIC DORSIFLEXOR

    K Number: K890200 · Decision Feb 3, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    113
    Registration Numbers
    113
    Same Product Code
    159
    Applicant Total
    5
    Review Days
    16

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    Basic Information

    Device Name
    PNEUMATIC DORSIFLEXOR
    K Number
    K890200
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    890.5380
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    Medical Flotation Systems, Inc.
    Date Received
    January 18, 1989
    Decision Date
    February 3, 1989
    Product Code
    BXB
    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
    BXB Exerciser, Powered

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