LogoFDA 510(k) Search
Search Filters

Search Results

Found 1 results

510(k) Data Aggregation

    K Number
    K971111
    Device Name
    TRI-TECH INC., EVACUATED BLOOD COLLECTION TUBE, GRAY STOPPER
    Manufacturer
    TRI-TECH, INC.
    Date Cleared
    1997-06-16

    (82 days)

    Product Code
    JKA
    Regulation Number
    862.1675
    Why did this record match?
    Applicant Name (Manufacturer) :

    TRI-TECH, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Plasma or whole blood collection device where glycolytic inhibition of the specimen is required.
    Device Description
    Evacuated Blood Collection Tube Gray Stopper
    Ask a Question

    Ask a specific question about this device

    Page 1 of 1