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510(k) Data Aggregation

    K Number
    K970827
    Device Name
    PRECISE
    Date Cleared
    1997-04-16

    (41 days)

    Product Code
    Regulation Number
    872.3710
    Why did this record match?
    Applicant Name (Manufacturer) :

    ALLAN SCHULMAN,D.D.S., M.S.

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