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

    H-O CAMERA

    K Number: K831832 · Decision Jul 7, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    3
    Review Days
    30

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    Basic Information

    Device Name
    H-O CAMERA
    K Number
    K831832
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Uni-Quatro Industries
    Date Received
    June 7, 1983
    Decision Date
    July 7, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    SU
    Third Party
    N

    Other Clearances by Uni-Quatro Industries

    K Number Device Name
    K863856 S-RAY CAMERA
    K831833 MX CAMERA