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510(k) Data Aggregation

    K Number
    K011518
    Device Name
    VITALSAT SERIES
    Date Cleared
    2002-11-15

    (547 days)

    Product Code
    Regulation Number
    870.2700
    Why did this record match?
    Applicant Name (Manufacturer) :

    BETA BIOMED SERVICES, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K003542
    Device Name
    PREAMP CABLE, MODEL B400-1011PA
    Date Cleared
    2001-04-06

    (140 days)

    Product Code
    Regulation Number
    870.2700
    Why did this record match?
    Applicant Name (Manufacturer) :

    BETA BIOMED SERVICES, INC.

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

    Ask a specific question about this device

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