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510(k) FDA Premarket Notification K243132

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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
06938396402754 K243132 000
06938396400491 K243132 000
06938396400552 K243132 000
06938396400569 K243132 000
06938396400965 K243132 000
06938396400972 K243132 000
06938396400989 K243132 000
06938396400996 K243132 000
06938396401016 K243132 000
06938396401023 K243132 000
06938396401030 K243132 000
06938396401047 K243132 000
06938396401054 K243132 000
06938396401061 K243132 000
06938396401078 K243132 000
06938396400484 K243132 000

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