BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

    Cryojet Plus (SHE-ACP001-1)

    K Number: K233416 · Decision Feb 6, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    478
    Registration Numbers
    480
    Same Product Code
    2867
    Applicant Total
    6
    Review Days
    119

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    Basic Information

    Device Name
    Cryojet Plus (SHE-ACP001-1)
    K Number
    K233416
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4810
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Beijing Sano Laser S&T Development Co.,Ltd
    Date Received
    October 10, 2023
    Decision Date
    February 6, 2024
    Product Code
    GEX
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    GEX Powered Laser Surgical Instrument

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