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510(k) Data Aggregation

    K Number
    K962243
    Device Name
    VASOTHERM
    Manufacturer
    Date Cleared
    1997-02-21

    (255 days)

    Product Code
    Regulation Number
    890.5290
    Why did this record match?
    Applicant Name (Manufacturer) :

    EHTI MEDICAL CORP.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K962703
    Device Name
    THEE THERMASTIM
    Manufacturer
    Date Cleared
    1997-02-21

    (224 days)

    Product Code
    Regulation Number
    890.5290
    Why did this record match?
    Applicant Name (Manufacturer) :

    EHTI MEDICAL CORP.

    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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