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510(k) Data Aggregation

    K Number
    K964452
    Device Name
    HEMATACHEK
    Manufacturer
    RICHMOND DIAGNOSTICS, INC.
    Date Cleared
    1997-02-20

    (106 days)

    Product Code
    GLK
    Regulation Number
    864.8625
    Why did this record match?
    Applicant Name (Manufacturer) :

    RICHMOND DIAGNOSTICS, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
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