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

    ALSITE MAGNIVISION

    K Number: K772228 · Decision Jan 3, 1978
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    28

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    Basic Information

    Device Name
    ALSITE MAGNIVISION
    K Number
    K772228
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Al Nyman & Son, Inc.
    Date Received
    December 6, 1977
    Decision Date
    January 3, 1978
    Advisory Committee
    Unknown
    Review Advisory Committee
    OP
    Third Party
    N