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Clinical Evaluation of the Safety and Performance of Fractional RF for the Treatment of Surgical Scars Following Breast Augmentation, Acromioplasty or Face Lift Protocol Identifying Number: CS0717 Principal
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Clinical evaluation is the assessment and analysis of clinical data pertaining to a medical device to verify its safety and performance.
Manufacturers of medical devices are required to file clinical evaluation forms.
Clinical evaluation forms must be filled out with accurate and up-to-date clinical data from relevant studies and trials.
The purpose of clinical evaluation forms is to ensure that medical devices on the market comply with regulatory requirements and are safe for use.
Clinical evaluation forms must include detailed information on the medical device, clinical data, patient populations, and any adverse events.
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