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510(k) FDA Premarket Notification K211329

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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 IdentifiersubmissionNumberSupplement
00810100050115 K211329 000
00810100050016 K211329 000
00810100050023 K211329 000
00810100050030 K211329 000
00810100050047 K211329 000
00850016172549 K211329 000
20810100050003 K211329 000
20810100050010 K211329 000
20810100050027 K211329 000
20810100050034 K211329 000
20810100050041 K211329 000
30850016172540 K211329 000
00810100050009 K211329 000

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