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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 IdentifiersubmissionNumberSupplement
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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