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

    DENLEY ANTHOS 2001 READER

    K Number: K894270 · Decision Aug 21, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    85
    Registration Numbers
    85
    Same Product Code
    257
    Applicant Total
    9
    Review Days
    60

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    Basic Information

    Device Name
    DENLEY ANTHOS 2001 READER
    K Number
    K894270
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.2300
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Denley Instruments, Inc.
    Date Received
    June 22, 1989
    Decision Date
    August 21, 1989
    Product Code
    JJQ
    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
    JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use

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    Other Clearances by Denley Instruments, Inc.

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    K915284 STACKING MICROPLATE WASHER
    K913567 WELLPREP 1
    K900599 MICROPLATE REAGENT DISPENSER
    K894272 DENLEY WELLDILL 3
    K894271 DENLEY WELLWASH 2 AND 4