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510(k) Data Aggregation

    K Number
    K951226
    Device Name
    VITALMAX 4000/MINIPACK 3100/3000
    Manufacturer
    Date Cleared
    1996-11-21

    (612 days)

    Product Code
    Regulation Number
    870.1110
    Why did this record match?
    Applicant Name (Manufacturer) :

    PACE TECH, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K953795
    Device Name
    VITALMAX 4100
    Manufacturer
    Date Cleared
    1996-07-01

    (322 days)

    Product Code
    Regulation Number
    868.1620
    Why did this record match?
    Applicant Name (Manufacturer) :

    PACE TECH, 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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