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510(k) Data Aggregation

    K Number
    K993143
    Device Name
    VITALITY SYSTEM
    Manufacturer
    Date Cleared
    1999-12-27

    (97 days)

    Product Code
    Regulation Number
    876.5020
    Reference & Predicate Devices
    N/A
    Predicate For
    N/A
    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
    Intended Use

    The Vitality System consists of a manual vacuum pump, a cylinder, cushion inserts, constriction ring loader, constriction rings, and lubricant. The Vitality System's intended use is to manage erectile dysfunction by allowing the creation of a full erection suitable for sexual activity. This is accomplished through the use of the manual vacuum pump to remove air from the cylinder, creating vacuum pressure within the cylinder. Blood is thereby drawn into the penis, causing it to become erect. The constriction ring is then placed around the base of the erect penis to restrict the outflow of blood. When activity is complete, the ring is removed from the base of the penis. This product is intended for over the counter use.

    Device Description

    The Vitality System consists of a manual vacuum pump, a cylinder, cushion inserts, constriction ring loader, constriction rings, and lubricant.

    AI/ML Overview

    This document is a 510(k) clearance letter for the Vitality System™, a manual vacuum pump device for erectile dysfunction. As such, it does not contain the information requested regarding acceptance criteria and a study proving the device meets those criteria.

    The letter confirms that the device is substantially equivalent to legally marketed predicate devices and is subject to general controls. It permits the device to be marketed.

    To answer the requested questions, one would need access to the 510(k) submission document itself, or other clinical trial data for the device if it exists.

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