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510k 231 wide

New England Journal of Medicine – Medical Devices – Balancing Regulation and Innovation

By Mesh Medical Device Newsdesk |

January 19, 2012 ~ In a letter to the Editor of the New England Journal of Medicine (NEJM), (here) January 19, 2012, Neil Feder, M.D. of the Project on Government Oversight writes about the 510(k) process that allows untested medical devices onto the market without premarket approval.

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