Device sector asked to comment on IOM's findings on 510(k) process

04/3/2011 |

The Institute of Medicine is seeking feedback from device industry representatives on its findings about the FDA's 510(k) clearance process. Dale Wahlstrom, who leads a group representing the medical device community in Minnesota, said the IOM asked him for suggestions of who in the industry could help review the institute's findings prior to its issuing a report this summer.

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