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

    KANDI-NUCLEAR MED. DATA ACQU.&INFO.

    K Number: K800835 · Decision May 28, 1980
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    2
    Review Days
    44

    Basic Information

    Device Name
    KANDI-NUCLEAR MED. DATA ACQU.&INFO.
    K Number
    K800835
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    KRUPP INTERNATIONAL, INC.
    Date Received
    April 14, 1980
    Decision Date
    May 28, 1980
    Advisory Committee
    Unknown
    Review Advisory Committee
    RA
    Third Party
    N

    Other Clearances by KRUPP INTERNATIONAL, INC.

    K Number Device Name
    K780090 DENTAL ALLOY