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510(k) Data Aggregation

    K Number
    K000599
    Device Name
    VITALOGRAPH BASE STATION
    Manufacturer
    Date Cleared
    2000-09-08

    (199 days)

    Product Code
    Regulation Number
    868.1840
    Why did this record match?
    Applicant Name (Manufacturer) :

    VITALOGRAPH, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K991412
    Device Name
    VITALOGRAPH MICRO
    Manufacturer
    Date Cleared
    2000-02-04

    (287 days)

    Product Code
    Regulation Number
    868.1860
    Why did this record match?
    Applicant Name (Manufacturer) :

    VITALOGRAPH, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    The Vitalograph Micro Spirometer is intended to measure, FVC, FEVI, PEF and FEV1% in patients with respiratory conditions such as Asthma, COPD, etc.
    Device Description
    Not Found
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