BEUDAMED
    FDA 510(k) Substantially Equivalent 🇮🇹 Italy

    MTH C/A MOBILE C ARM

    K Number: K827993 · Decision Sep 13, 1982
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    7
    Review Days
    20

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    Basic Information

    Device Name
    MTH C/A MOBILE C ARM
    K Number
    K827993
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    General Medical Merate S.P.A
    Date Received
    August 24, 1982
    Decision Date
    September 13, 1982
    Advisory Committee
    Unknown
    Review Advisory Committee
    RA
    Third Party
    N

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    K041605 PRECISION RXI ANALOG X-RAY SYSTEM
    K881386 X-RAY GENERATING SYSTEM TF 1000