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510(k) Data Aggregation

    K Number
    K980082
    Date Cleared
    1998-03-04

    (54 days)

    Product Code
    Regulation Number
    880.5430
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The J-Tip Needleless Injector system is used for the subcutaneous administration of medications which are appropriate to deliver by jet injection.

    Device Description

    J-Tip Needles Injector

    AI/ML Overview

    Apologies, but the provided text from the FDA 510(k) letter for the "J-Tip Needleless Injector" does not contain the information requested regarding acceptance criteria and details of a study proving device performance.

    The document is a substantial equivalence determination letter, which means the FDA has determined that the J-Tip Needleless Injector is as safe and effective as a legally marketed predicate device. This letter typically does not include the detailed study methodology, acceptance criteria, or performance data that would be found in a 510(k) summary or the actual submission itself.

    Therefore, I cannot provide the specific details you've asked for based on the input document, such as:

    1. A table of acceptance criteria and reported device performance.
    2. Sample sizes or data provenance.
    3. Number or qualifications of experts for ground truth.
    4. Adjudication method.
    5. MRMC comparative effectiveness study results.
    6. Standalone performance details.
    7. Type of ground truth used.
    8. Training set details.
    9. Ground truth establishment for the training set.

    The letter focuses on the regulatory decision and the device's classification, not the technical study details.

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