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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
20847212008431	K230002	000
20847212008424	K230002	000
20847212008417	K230002	000
20847212008400	K230002	000
20847212008516	K230002	000
20847212008509	K230002	000
20847212008493	K230002	000
20847212008486	K230002	000
00840369321718	K230002	000

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