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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
06945121414777	K223570	000
06945121414609	K223570	000
06945121414579	K223570	000
06945121414562	K223570	000
06945121414555	K223570	000
06945121414548	K223570	000
06945121414531	K223570	000
06945121414524	K223570	000

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