BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

    TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVE

    K Number: K902958 · Decision Nov 1, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    130
    Registration Numbers
    130
    Same Product Code
    264
    Applicant Total
    5
    Review Days
    119

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    Basic Information

    Device Name
    TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVE
    K Number
    K902958
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.2800
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Board of Directors, Albert Browne , Ltd.
    Date Received
    July 5, 1990
    Decision Date
    November 1, 1990
    Product Code
    JOJ
    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
    JOJ Indicator, Physical/Chemical Sterilization Process

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    Other Clearances by Board of Directors, Albert Browne , Ltd.

    K Number Device Name
    K971971 BROWNE TST SINGLE USE BOWIE-DICK TYPE TEST PACK
    K970918 BROWNE STEAM INDICATOR
    K932057 BROWNE TST SINGLE USE BOWIE DICK TYPE TEST PACK
    K922481 BROWNE GA INDICATOR USE IN 2% ACTIV GLUTARALDEHYDE