510(k) FDA Premarket Notification K222570

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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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Correspondent

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
04260102139299	K222570	000
04260102139275	K222570	000
04260102139244	K222570	000

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