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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
08809260475038	K233153	000
08809260473676	K233153	000
08809260473713	K233153	000
08809260473942	K233153	000
08809260473980	K233153	000
08809260474017	K233153	000
08809260474697	K233153	000
08809260474727	K233153	000
08809260474987	K233153	000
08809260474994	K233153	000
08809260473669	K233153	000

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