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

    PODIOSCOPE BY ARROW

    K Number: K827069 · Decision Feb 18, 1982
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    2
    Review Days
    31

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    Basic Information

    Device Name
    PODIOSCOPE BY ARROW
    K Number
    K827069
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Arrow X-Ray Corp.
    Date Received
    January 18, 1982
    Decision Date
    February 18, 1982
    Advisory Committee
    Unknown
    Review Advisory Committee
    RA
    Third Party
    N

    Other Clearances by Arrow X-Ray Corp.

    K Number Device Name
    K820119 PODIOSCOPE BY ARROW