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MDUFMA Blue Book Memos

Section 206 of the Medical Device User Fee and Modernization Act (MDUFMA) (New section 502(f) of the Federal Food, Drug, and Cosmetic Act) Electronic Labeling for Prescription Devices Intended for Use in Health Care Facilities - #G03-1

Updated 4/4/2003

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Center for Devices and Radiological Health / CDRH

Web page created April 4, 2003