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 'U.S. FDA 510(k) Document' 
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U.S. FDA 510(k) Document
A guidance document available from the 'Center for Devices and Radiological Health, U.S. Food and Drug Administration', which provides information for manufacturers seeking U.S. marketing clearance of diagnostic ultrasound systems and transducers.
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 [last update: 2023-11-06 01:42:00]