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510(k) FDA Premarket Notification K243173

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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
00816847022750 K243173 000
00816847022743 K243173 000
00816847022736 K243173 000

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