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510(k) FDA Premarket Notification K243178

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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
06938396401443 K243178 000
06938396401283 K243178 000
06938396401337 K243178 000
06938396401344 K243178 000
06938396401351 K243178 000
06938396401368 K243178 000
06938396401375 K243178 000
06938396401382 K243178 000
06938396401399 K243178 000
06938396401405 K243178 000
06938396401412 K243178 000
06938396401429 K243178 000
06938396401436 K243178 000
06938396400347 K243178 000

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