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510(k) FDA Premarket Notification K232736

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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
00812203030667 K232736 000
00812203030759 K232736 000
00812203030766 K232736 000
00812203030773 K232736 000
00812203030728 K232736 000
00812203030711 K232736 000
00812203030735 K232736 000
00812203030674 K232736 000
00812203030681 K232736 000
00812203030643 K232736 000
00812203030650 K232736 000
00812203030797 K232736 000

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