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510(k) Data Aggregation

    K Number
    K050557
    Device Name
    AMT NANOCATH
    Date Cleared
    2005-05-27

    (85 days)

    Product Code
    Regulation Number
    868.5120
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    AMT NANOCATH

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The AMT NanoCath™ epidural catheter is intended for administration of local anesthetics into the epidural space to provide continuous epidural caudal anesthesia for up to 72 hours

    Device Description

    The AMT NanoCath is comprised of a tightly coiled stainless steel, covered over most of its length with polvethylene terphthalate. The tip of the catheter is welded into a smooth cover to which is welded a safety ribbon of stainless steel. A stylet of stainless with a plastic handle made of delrin or polycarbonate fits inside the catheter. The catheter is available in 19 - 21 gauge, in lengths of 30 to 90 cm. The wire coil has an outer diameter from 0.8 to 1.0 mm. The NanoCath was compared with substantially equivalent devices in fatigue tests and shown equivalent.

    AI/ML Overview

    The provided text does not contain information about acceptance criteria and a study proving a device meets these criteria in the context of an AI/algorithm-based medical device. Instead, it is a 510(k) summary for the AMT NanoCath™ epidural catheter, focusing on its substantial equivalence to predicate devices based on material characteristics, intended use, and bench testing.

    Therefore, I cannot populate the table or answer the specific questions related to acceptance criteria, study design, expert involvement, or AI performance. The document describes a traditional medical device submission, not an AI/ML medical device submission.

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