The Food and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH) announced last week about a new actions for the 510(K) program , which is the commonly-used pathway to market for medical devices. To see the program please use the attached link.
http://www.integrity-c-s.co.il/uploads/New actions for the 510(K) program(1).pdf
http://www.integrity-c-s.co.il/uploads/New actions for the 510(K) program(1).pdf
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