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

    BIOCIRCUITS IOS (IN-OFFICE SYSTEM)

    K Number: K952719 · Decision Nov 22, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    51
    Registration Numbers
    51
    Same Product Code
    37
    Applicant Total
    8
    Review Days
    160

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    Basic Information

    Device Name
    BIOCIRCUITS IOS (IN-OFFICE SYSTEM)
    K Number
    K952719
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.2560
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Biocircuits Corp.
    Date Received
    June 15, 1995
    Decision Date
    November 22, 1995
    Product Code
    KHO
    Advisory Committee
    Clinical Chemistry
    Review Advisory Committee
    CH
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KHO Fluorometer, For Clinical Use

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    Other Clearances by Biocircuits Corp.

    K Number Device Name
    K981634 BIOCIRCUITS IOS PROSTATE SPECIFIC ANTIGEN (PSA) TEST CARTRIDGES, BIOCIRCUITS IOS PSA CONTROLS
    K980819 BIOCIRCUITS IOS FREE THYROXINE (FT4) TEST CARTRIDGES BIOCIRCUITS IOS CONTROLS
    K963770 BIOCIRCUITS IOS QUANTITATIVE HCG TEST CARTRIDGES/BIOCIRCUITS IOS IMMUNOASSAY CONTROLS
    K961566 BIOCIRCUITS IOS TSH TEST CARTRIDGES/THYROID CONTROLS
    K961792 BIOCIRCUITS IOS SERUM PREGNANCY TEST CARTRIDGES/IMMUNOASSAY CONTROLS
    K952751 BIOCIRCUITS IOS T4/TU TEST CARTRIDGES
    K953837 BIOCIRCUITS IOS T4 TEST CARTRIDGE