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

    YEAST-PALETTE TM

    K Number: K790991 · Decision Jun 22, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    12
    Registration Numbers
    12
    Same Product Code
    15
    Applicant Total
    2
    Review Days
    24

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    Basic Information

    Device Name
    YEAST-PALETTE TM
    K Number
    K790991
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    866.2660
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Micro-Palettes, Inc.
    Date Received
    May 29, 1979
    Decision Date
    June 22, 1979
    Product Code
    JXB
    Advisory Committee
    Microbiology
    Review Advisory Committee
    MI
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JXB Kit, Identification, Yeast

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    Other Clearances by Micro-Palettes, Inc.

    K Number Device Name
    K790992 PSEUDO-PALETTE TM