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510(k) Data Aggregation

    K Number
    K963510
    Device Name
    APREMA I - ALTERNATING PRESSURE AIR FLOTATION MATTRESS SYSTEM
    Date Cleared
    1996-11-26

    (84 days)

    Product Code
    Regulation Number
    880.5550
    Why did this record match?
    Applicant Name (Manufacturer) :

    MELLEN AIR MFG., INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K961129
    Device Name
    AREMA II
    Date Cleared
    1996-04-17

    (27 days)

    Product Code
    Regulation Number
    880.5550
    Why did this record match?
    Applicant Name (Manufacturer) :

    MELLEN AIR MFG., 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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