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510(k) Data Aggregation

    K Number
    K963669
    Manufacturer
    Date Cleared
    1996-12-12

    (90 days)

    Product Code
    Regulation Number
    882.1835
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    GRASS MODEL 15 NEURODATA AMPLIFIER SYSTEM

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

    Not Found

    Device Description

    The Model 15 combines up to 32 of the P511 amplifier circuits (in banks of 4) in a single enclosure and replaces the P511 manual switches with solid-state switches that are controlled via a standard RS-232 serial port. The Model 15 relies on the essential safely features of the P511 amplifier capacity-coupled patient circuit and safety-extra-low-voltage operation (12VDC) and improves on the safety of the P511 by isolating the patient applied circuits from the enclosure (earth).

    AI/ML Overview

    This K96 3669 document is a 510(k) summary for the Grass® Model 15 Neurodata Amplifier System. It focuses on demonstrating substantial equivalence to pre-existing devices rather than presenting a study proving the device meets specific performance acceptance criteria.

    Therefore, the requested information regarding acceptance criteria, study design, sample sizes, ground truth, and expert adjudication cannot be extracted from the provided text. The document primarily describes the device, its classification, and its equivalence to older Grass models (P511) and the Melville Diagnostics MMC Series, highlighting design and safety similarities.

    There is no mention of a clinical or performance study with defined acceptance criteria, test sets, training sets, or expert evaluations. The closest relevant information is the assertion that the Model 15 shares essential design, performance, and safety characteristics with the older, FDA-listed Grass P511 amplifier.

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