510(k) FDA Premarket Notification K233722

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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
04540217071395	K233722	000
04540217071388	K233722	000
04540217071371	K233722	000
04540217071364	K233722	000
04540217071357	K233722	000
04540217071340	K233722	000
04540217071333	K233722	000
04540217071326	K233722	000
04540217071319	K233722	000

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