On the recordJuly 27, 2011
the review of the 510(k) products. It's become particularly burdensome, causing product approval delays and the frustration for the manufacturers, providers, and obviously the patients.
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congress.govKay Hagan: “the review of the 510(k) products. It's become particularly burdensome, causing product approval delays and the…”
Editor's note · Context
Senator Hagan expresses concerns about delays in medical device approvals affecting jobs and innovation.
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