GEHC Traditional 510(k) Premarket Notification Template

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Date: 2014-10-06 09:56:06 Medical device Premarket approval Surgery Infection control Federal Food Drug and Cosmetic Act Center for Devices and Radiological Health Medicine Health Food and Drug Administration		GEHC Traditional 510(k) Premarket Notification Template Add to Reading List Source URL: www.accessdata.fda.gov Download Document from Source Website File Size: 175,51 KB Share Document on Facebook

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