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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
00850042929148	K223722	000
00860011521228	K223722	000
00850042929322	K223722	000
00850042929339	K223722	000
00850042929384	K223722	000
00850042929391	K223722	000
00860004687535	K223722	000
00860004687542	K223722	000
00860004687559	K223722	000
10875011000311	K223722	000
00850042929261	K223722	000
00850042929278	K223722	000
00850042929193	K223722	000
00850042929209	K223722	000
00810115891598	K223722	000
00810115891703	K223722	000
00850042929131	K223722	000
00860011521204	K223722	000

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