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Technology / Unique Device Identification / Center for Devices and Radiological Health / Medical device / Premarket approval / Adverse event / Title 21 CFR Part 11 / Structured Product Labeling / Food and Drug Administration / Medicine / Health
Technology
Unique Device Identification
Center for Devices and Radiological Health
Medical device
Premarket approval
Adverse event
Title 21 CFR Part 11
Structured Product Labeling
Food and Drug Administration
Medicine
Health

FDA’s Home Use Medical Device Initiative

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Source URL: www.fda.gov

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