BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    BEESON AUTOMADDAK FEEDER

    K Number: K770169 · Decision Jan 28, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    78
    Registration Numbers
    78
    Same Product Code
    31
    Applicant Total
    6
    Review Days
    3

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    Basic Information

    Device Name
    BEESON AUTOMADDAK FEEDER
    K Number
    K770169
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    890.5050
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    Techhnilab Instruments, Inc.
    Date Received
    January 25, 1977
    Decision Date
    January 28, 1977
    Product Code
    ILC
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

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

    Product Code Device Name
    ILC Utensil, Eating

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