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.govThe 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.
Senator Hagan expresses concerns about delays in medical device approvals affecting jobs and innovation.
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