Scrutinizing 510(k)s: Critical Voices Get Heard In Congress - Medical Devices Today

Medical Devices Today: Scrutinizing 510(k)s: Critical Voices Get Heard In Congress: "Consumer advocacy groups have recently stepped up efforts to publicly scrutinize FDA's 510(k) premarket notification process for devices and push for a higher burden of proof for getting the products to market. Consumer advocacy groups have recently stepped up efforts to publicly scrutinize FDA's 510(k) premarket notification process for devices and push for a higher burden of proof for getting the products to market. "