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510(k) Data Aggregation

    K Number
    K011787
    Manufacturer
    Date Cleared
    2001-07-06

    (28 days)

    Product Code
    Regulation Number
    876.4300
    Reference & Predicate Devices
    N/A
    Why did this record match?
    Device Name :

    PRECISION TUNA OFFICE SYSTEM WITH NO RECTAL TEMPERATURE MONITORING TAPE

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

    The TUNA Office System is intended for use in the treatment of symptoms due to urinary outflow obstruction secondary to Benign Prostatic Hyperplasia (BPH) in men over the age of 50 with prostate sizes between 20 and 50 cc.

    Device Description

    Precision™ TUNA® Office System with Model 6800 Cartridge, Model 6198 Handle, Model 7800 RF Generator (with no rectal temperature monitoring tape)

    AI/ML Overview

    This document is a 510(k) clearance letter from the FDA, which determines substantial equivalence to a predicate device. It does not contain information about acceptance criteria, study details, or device performance metrics typically found in a clinical study report or a detailed pre-market submission.

    Therefore, I cannot provide the requested information from the provided text. The document primarily focuses on regulatory approval and classification for the "Precision™ TUNA® Office System."

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