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510(k) Data Aggregation

    K Number
    K965241
    Date Cleared
    1997-02-28

    (79 days)

    Product Code
    Regulation Number
    878.4400
    Reference & Predicate Devices
    Why did this record match?
    Device Name :

    BIPOLAR SUCTION COAGULATOR

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

    The Bipolar Suction Coagulator (Angled) is a disposable device, designed to be used in soft tissue surgical procedures that require slow to rapid fluid evacuation and low energy output for the coagulation of the tissue i.e., neurosurgery, endoscopic, sinusoidial, ENT, OB-GYN and plastic surgery.

    Device Description

    The Bipolar Suction Coagulator (Angled) is a disposable device, designed to be used in soft tissue surgical procedures that require slow to rapid fluid evacuation and low energy output for the coagulation of the tissue i.e., neurosurgery, endoscopic, sinusoidial, ENT, OB-GYN and plastic surgery.

    AI/ML Overview

    The provided text is a summary of safety and effectiveness for a Bipolar Suction Coagulator. It details various safety and performance standards met by the device. However, it does not contain the specific information requested about acceptance criteria, device performance metrics (sensitivity, specificity, accuracy, etc.), details of a study (sample size, data provenance, ground truth establishment, expert qualifications), or comparative effectiveness studies with AI or standalone algorithm performance.

    The document primarily focuses on:

    • Intended Use: Soft tissue surgical procedures requiring fluid evacuation and low-energy coagulation.
    • Biological Safety: Materials tested according to ISO 10993-1.
    • Sterilization Safety: Validated to a SAL of 10-6 using EtO sterilization.
    • Performance Testing: Compliance with IEC 601-1-2, IEC 601-2-2, and ANSI/AAMI HF 18.
    • Substantial Equivalence: To Bipolar Suction Coagulator, K960455.

    Therefore, I cannot populate the requested table or answer the specific questions because the necessary data is not present in the provided input. This document describes regulatory compliance and testing for a physical medical device, not the performance metrics of a diagnostic or AI-driven system.

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    K Number
    K960455
    Date Cleared
    1996-02-27

    (28 days)

    Product Code
    Regulation Number
    878.4400
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    BIPOLAR SUCTION COAGULATOR

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use
    Device Description
    AI/ML Overview
    Ask a Question

    Ask a specific question about this device

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