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

    RATEMINDER

    K Number: K812233 · Decision Aug 25, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    6
    Registration Numbers
    6
    Same Product Code
    59
    Applicant Total
    2
    Review Days
    14

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    Basic Information

    Device Name
    RATEMINDER
    K Number
    K812233
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5725
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Anatros Corp.
    Date Received
    August 11, 1981
    Decision Date
    August 25, 1981
    Product Code
    LDR
    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
    LDR Controller, Infusion, Intravascular, Electronic

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    Other Clearances by Anatros Corp.

    K Number Device Name
    K833520 RATEMINDER II SPECIALTY CARE