510(k) FDA Premarket Notification K234147

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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
00811099014300	K234147	000
00811099014287	K234147	000
00811099014270	K234147	000
00811099014263	K234147	000
00811099014256	K234147	000
00081109901429	K234147	000
00811099014294	K234147	000

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