510(k) FDA Premarket Notification K221861

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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
06973031299948	K221861	000
06973031299528	K221861	000
06973031299535	K221861	000
06973031299542	K221861	000
06973031299825	K221861	000
06973031299832	K221861	000
06973031299962	K221861	000
06973031299672	K221861	000
06973031299955	K221861	000
06973031299689	K221861	000
06973031299696	K221861	000
06973031299702	K221861	000
06973031299719	K221861	000
06973031299931	K221861	000
06973031299511	K221861	000

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