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Home » U.S. FDA Device Center Launches eSubmission Pilot for Traditional 510(k)s
U.S. FDA Device Center Launches eSubmission Pilot for Traditional 510(k)s
Devicemakers will be able to submit traditional 510(k)s electronically to two branches in the U.S. Food and Drug Administration’s Center for Devices and Radiological Health, under an experimental program announced May 1.
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