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510(k) Data Aggregation

    K Number
    K011967
    Manufacturer
    Date Cleared
    2002-01-23

    (212 days)

    Product Code
    Regulation Number
    880.5200
    Reference & Predicate Devices
    Predicate For
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Heparin Lock Flush Solution, USP syringes are intended for use in maintaining patency of vascular access devices (VAD'S).

    Device Description

    Heparin Lock Flush Solution, USP BD Pre-Filled Heparin Lock Flush Syringe. Product sizes/reorder numbers: The following sizes/reorder numbers of the Heparin Lock Flush Solution, USP syringes to be offered are:

    BD Cat. #Description
    306509Heparin, 10u/mL, 6mL Fill In 10mL Syringe
    306510Heparin, 10u/mL, 5mL Fill In 10mL Syringe
    306511Heparin, 10u/mL, 5mL Fill In 5mL Syringe
    306521Heparin, 10u/mL, 3mL Fill In 10mL Syringe
    306512Heparin, 10u/mL, 3mL Fill In 3mL Syringe
    306527Heparin, 10u/mL, 2mL Fill In 3mL Syringe
    306513Heparin, 100u/mL, 5mL Fill In 10mL Syringe
    306514Heparin, 100u/mL, 3mL Fill In 10mL Syringe
    306515Heparin, 100u/mL, 5mL Fill In 5mL Syringe
    306516Heparin, 100u/mL, 3mL Fill In 5mL Syringe
    306517Heparin, 100u/mL, 3mL Fill In 3mL Syringe
    306528Heparin, 100u/mL, 2mL Fill In 3mL Syringe
    306525Heparin, 10u/mL, 5mL Fill In 10mL Syringe With Blunt Plastic Cannula
    306531Heparin, 100u/mL, 5mL Fill In 10mL Syringe With Blunt Plastic Cannula
    306529Heparin, 100u/mL, 5mL Fill In 5mL Syringe With Blunt Plastic Cannula
    306537SASH Kit (2 - 0.9% Sodium Chloride Syringes and 1 - 100u/mL Heparin Lock Flush Syringe), 5mL Fill In 10mL Syringe - 100u/mL Heparin
    306538SASH Kit (2 - 0.9% Sodium Chloride Syringes and 1 - 10u/mL Heparin Lock Flush Syringe), 3mL Fill In 3mL Syringe - 10u/mL Heparin
    306539SASH Kit (2 - 0.9% Sodium Chloride Syringes and 1 - 100u/mL Heparin Lock Flush Syringe), 3mL Fill In 5mL Syringe - 100u/mL Heparin

    The Heparin Lock Flush Solution, USP syringe contains sterile flush (0.9% Sodium Chloride Injection, USP and Heparin Sodium 10 and 100U/mL solution as does the predicate devices). The Heparin Lock Flush Solution, USP syringe has a sterile solution contents and fluid path as do the predicate devices. The Heparin Lock Flush Solution, USP syringe is aseptically filled as the predicate device, BD Preefil™. The Heparin Lock Flush Solution, USP syringe is a three-piece piston design as are the predicate devices, BD Preefil™and the Baxter Heparin Lock Flush syringe. The Heparin Lock Flush Solution, USP syringe barrel is molded from polypropylene as are the predicate devices, BD Preefil™and the Baxter Heparin Lock Flush syringe. The Heparin Lock Flush Solution, USP syringe has a similar package unit design as the predicate device, BD Preefil™.

    AI/ML Overview

    This document is a 510(k) premarket notification for a medical device – specifically, a pre-filled heparin lock flush syringe. These types of regulatory submissions do not typically include studies or data proving acceptance criteria in the manner one would see for AI/ML-based diagnostic devices.

    Instead, the submission focuses on demonstrating "substantial equivalence" to predicate devices already on the market. This means the manufacturer is asserting that their new device is as safe and effective as existing legally marketed devices, based on similar intended use, technology, and performance characteristics, rather than independent performance studies with acceptance criteria.

    Therefore, the requested information about acceptance criteria, study details, sample sizes, ground truth establishment, expert adjudication, MRMC studies, and standalone performance is not present in the provided text.

    The document states:

    • Intended Use: "Heparin Lock Flush Solution, USP syringes are intended for use in maintaining patency of vascular access devices (VAD'S)."
    • Equivalence Determination: The manufacturer compares their device to predicate devices based on elements like solution contents, sterility, filling process, design, and materials (e.g., "The Heparin Lock Flush Solution, USP syringe contains sterile flush... as does the predicate devices").

    Because this is a substantial equivalence claim for a physical medical device, not an AI/ML algorithm, the requested study details are not applicable.

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