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Negative Pressure System Becomes First FDA-Indicated Device to Aid in Reduction of SSIs
05/16/2019
KCI, an Acelity Company (San Antonio, TX), announced that PREVENA™ Incision Management System has become the first and only FDA-indicated negative pressure device to aid in the reduction of superficial surgical site infections (SSIs) in patients at a high risk for post-operative infections in Class I and II wounds. This device is the first disposable negative pressure system that was designed specifically for the management of closed surgical incisions by removing fluid away from the surgical incision with continuous negative pressure.
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