**OR Technology Section[removed]k) Summary

First Page		Document Content
Date: 2013-12-09 11:45:21 Food law Medical equipment Pharmaceutical industry Radiography Medical device Federal Food Drug and Cosmetic Act Konica Minolta Title 21 of the Code of Federal Regulations Premarket approval Medicine Technology Food and Drug Administration		**OR Technology Section[removed]k) Summary Add to Reading List Source URL: www.accessdata.fda.gov Download Document from Source Website File Size: 157,96 KB Share Document on Facebook

	Microsoft PowerPoint - ditto DocID: 1gc7K - View Document
	Microsoft PowerPoint - ditto DocID: 1g6Me - View Document
	Federal Register / Vol. 80, NoWednesday, May 6, Notices Submit electronic comments on the draft guidance to http:// www.regulations.gov. Submit written comments to the Division of Dockets Management (HFA– DocID: 1aGhA - View Document
	This document is scheduled to be published in the Federal Register onand available online at http://federalregister.gov/a, and on FDsys.govP DEPARTMENT OF HEALTH AND HUMAN SERVICES DocID: 1akUI - View Document
	CLEAN version with no appendices DocID: 1ahmv - View Document