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The following data is part of a premarket notification filed by with the FDA for .

Pre-market Notification Details

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NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
06936666559269	K232505	000
16936666559280	K232505	000
16936666559297	K232505	000
16936666559303	K232505	000
16936666559310	K232505	000
16936666559327	K232505	000
16936666559334	K232505	000
16936666559341	K232505	000
16936666559358	K232505	000
16936666559365	K232505	000
16936666559372	K232505	000
16936666559389	K232505	000
16936666559396	K232505	000
16936666559402	K232505	000
16936666559419	K232505	000
16936666559273	K232505	000

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