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510(k) Data Aggregation

    K Number
    K962829
    Date Cleared
    1997-10-16

    (475 days)

    Product Code
    Regulation Number
    870.1200
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    HARMAC BALLOON ANGIOGRAPHIC CATHETER

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

    The Balloon Angiographic catheter is indicated for use in right heart catheterization for cardiac angiography, and measurement of the right heart and pulmonary artery pressures. It can be used to inject radiopaque media and measure pressures in any chamber or vessel that can be entered from the right heart.

    Device Description

    Harmac Balloon Angiographic Catheter

    AI/ML Overview

    This document is a 510(k) clearance letter from the FDA for a medical device (Harmac Balloon Angiographic Catheter). It does not contain any information about acceptance criteria, device performance reporting, or a study that proves the device meets acceptance criteria.

    The letter explicitly states that the FDA has reviewed the Section 510(k) notification of intent to market the device and determined it is "substantially equivalent" to devices marketed prior to May 28, 1976. This is a regulatory pathway for medical devices that are similar to existing legally marketed devices, and often does not require new clinical studies demonstrating safety and effectiveness compared to devices undergoing a Premarket Approval (PMA) pathway.

    Therefore, I cannot extract the requested information from the provided text. The document is solely a regulatory clearance for market entry based on substantial equivalence, not a performance study report.

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