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

    SMART-WELL INCUBATOR

    K Number: K122362 · Decision Mar 26, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    42
    Registration Numbers
    42
    Same Product Code
    205
    Applicant Total
    9
    Review Days
    232

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    Basic Information

    Device Name
    SMART-WELL INCUBATOR
    K Number
    K122362
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    880.2800
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Mesa Laboratories, Inc.
    Date Received
    August 6, 2012
    Decision Date
    March 26, 2013
    Product Code
    FRC
    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
    FRC Indicator, Biological Sterilization Process

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