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Home » Minnesota Device Group Files Citizen Petition to Prevent FDA From Unlawfully Changing 510(k)
Minnesota Device Group Files Citizen Petition to Prevent FDA From Unlawfully Changing 510(k)
January 7, 2013
A Minneapolis law firm has filed a joint petition on behalf of a group of pre-revenue, small and midsized device companies, venture capitalists and inventing physicians that aims to prevent the FDA from unlawfully changing how the 510(k) program operates. MedCity News
