Reprocessing Industry Group Applauds GAO Report Findings

"Medical device reprocessing, as the GAO again confirms, is stringently regulated by the Food and Drug Administration (FDA),” Vukelich says. “Twice in eight years GAO has looked at the practice of reprocessing ‘single-use’ devices (SUDs) and found no evidence of increased risk to patients.”

To read the complete story pleae click on the link.