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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
B675ONEVEOG1	K233403	000
B675MM0	K233403	000
B675ONEAUX1	K233403	000
B675ONEDU0	K233403	000
B675ONEECG1	K233403	000
B675ONEEMG1	K233403	000
B675ONEESB1	K233403	000
B675ONEHEOG1	K233403	000
B675ONEHU1	K233403	000
B675ONEREF1	K233403	000
B675DC0	K233403	000

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