Category US FDA Medical Device, 510(k) Submission, 510(k) for a Change, Medical Device approval, FDA 510K recommendations, 510K requirements, device safety and effectiveness, device safety, QS regulation, CAPA, FDA review and approval, FDA 510K document.
Deadline: April 10, 2017 | Date: April 11, 2017
Venue/Country: CA, U.S.A
Updated: 2017-03-20 18:14:49 (GMT+9)
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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