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Technology / Premarket approval / Medical device / Prescription Drug User Fee Act / Investigational Device Exemption / Structured Product Labeling / Unique Device Identification / Food and Drug Administration / Medicine / Health
Date: 2014-05-29 06:03:01
Technology
Premarket approval
Medical device
Prescription Drug User Fee Act
Investigational Device Exemption
Structured Product Labeling
Unique Device Identification
Food and Drug Administration
Medicine
Health

[removed]Federal Register / Vol. 79, No[removed]Thursday, May 29, [removed]Notices to meet current standards, the Agency will advise ANDA applicants to submit

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