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

    ULTRA PULSATOR

    K Number: K831472 · Decision Jul 26, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    4
    Review Days
    81

    Basic Information

    Device Name
    ULTRA PULSATOR
    K Number
    K831472
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    MEDELCO LTD.
    Date Received
    May 6, 1983
    Decision Date
    July 26, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    PM
    Third Party
    N

    Other Clearances by MEDELCO LTD.

    K Number Device Name
    K853767 FLOSPIK
    K831473 ULTRA PULSATOR MF
    K831474 MINI PULSATOR