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

    MINIATURE ASCENDING PAPER CHROMATO-

    K Number: K760908 · Decision Nov 19, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    3
    Registration Numbers
    3
    Same Product Code
    4
    Applicant Total
    1
    Review Days
    24

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    Basic Information

    Device Name
    MINIATURE ASCENDING PAPER CHROMATO-
    K Number
    K760908
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.2270
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Ackerman Nuclear, Inc.
    Date Received
    October 26, 1976
    Decision Date
    November 19, 1976
    Product Code
    DPA
    Advisory Committee
    Clinical Chemistry
    Review Advisory Committee
    TX
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DPA Apparatus, General Use, Thin Layer Chromatography

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