BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    LIQUID NITROGEN SPRAY UNIT

    K Number: K772232 · Decision Dec 15, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    83
    Registration Numbers
    83
    Same Product Code
    261
    Applicant Total
    2
    Review Days
    16

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    Basic Information

    Device Name
    LIQUID NITROGEN SPRAY UNIT
    K Number
    K772232
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4350
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Gilmore Liquid Air Co.
    Date Received
    November 29, 1977
    Decision Date
    December 15, 1977
    Product Code
    GEH
    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
    GEH Unit, Cryosurgical, Accessories

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    Other Clearances by Gilmore Liquid Air Co.

    K Number Device Name
    K801921 GCS-79