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

    CASTLE 7515 UTENSIL/GLASSWARE WASHER

    K Number: K844089 · Decision Jan 14, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    10
    Applicant Total
    21
    Review Days
    84

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    Basic Information

    Device Name
    CASTLE 7515 UTENSIL/GLASSWARE WASHER
    K Number
    K844089
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.6991
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Castle Co.
    Date Received
    October 22, 1984
    Decision Date
    January 14, 1985
    Product Code
    LDS
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LDS Device, Pasteurization, Hot Water

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