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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
14953170421348	K240617	000
04953170200311	K240617	000
04953170200373	K240617	000
04953170209154	K240617	000
04953170415111	K240617	000
04953170415128	K240617	000
04953170415135	K240617	000
04953170415142	K240617	000
04953170415159	K240617	000
04953170415166	K240617	000
04953170415173	K240617	000
14953170421331	K240617	000
04953170200298	K240617	000

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