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Medical News & Perspectives |

FDA Ponders Regulation and Innovation

Rebecca Voelker
JAMA. 2011;305(15):1523-1524. doi:10.1001/jama.2011.493.
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Most hip implants, ventilators, nonimplantable infusion pumps—even a radiology app for mobile phones—have traveled the same road from an inventor's mind to a physician's hands. These devices and thousands of other common medical products reach the market through a federal pathway known as the 510(k) clearance process.

Now 35 years old, the 510(k) process was created as a way for low- to moderate-risk medical devices such as tongue depressors or hearing aids to pass muster with the US Food and Drug Administration (FDA), yet bypass the stringent regulatory requirements that apply to devices considered high risk because their failure or misuse can lead to serious injury or death.

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The US Food and Drug Administration says that modernizing its 510(k) clearance process will spur much-needed innovation in medical devices and keep jobs from going overseas.

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