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510(k) Data Aggregation

    K Number
    K962180
    Device Name
    CATH SEAL
    Date Cleared
    1996-11-07

    (154 days)

    Product Code
    Regulation Number
    870.1340
    Why did this record match?
    Applicant Name (Manufacturer) :

    UNIVERSAL MEDICAL INSTRUMENT CORP.

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