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Home » U.S. FDA Exempts 30 Devices From Premarket Requirements
U.S. FDA Exempts 30 Devices From Premarket Requirements
August 17, 2011
The U.S. Food and Drug Administration (FDA) is exempting 30 different types of diagnostic and radiology devices from premarket requirements and has released a guidance outlining the affected products.
International Medical Device Regulatory Monitor
International Medical Device Regulatory Monitor
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