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510(k) Data Aggregation

    K Number
    K000572
    Device Name
    E.N.S.I. SYRINGE
    Manufacturer
    TRI-JECT INTL. CORP.
    Date Cleared
    2000-02-24

    (2 days)

    Product Code
    MEG
    Regulation Number
    880.5860
    Why did this record match?
    Applicant Name (Manufacturer) :

    TRI-JECT INTL. CORP.

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