By Jan K. Seigel | Published November 24, 2010 | Posted in Medical Malpractice | Tagged Tags: 501(k) approval, FDA, medical devices, PMA, premarket approval, Public Citizen | Leave a comment
Recently, the FDA issued proposed changes to the approval processes for medical devices. The changes come on the heels of a September 2009 report in which the FDA accused some of its own top regulators of caving in to political pressure when approving some products. In July, the advocacy group Public Citizen released a report Read More
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