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510(k) FDA Premarket Notification K231172

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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
05056139246791 K231172 000
05056139245749 K231172 000
05056139245732 K231172 000
05056139245725 K231172 000
05056139245701 K231172 000
05056139245169 K231172 000
05056139245152 K231172 000
05056139244964 K231172 000
05056139244957 K231172 000
05056139245855 K231172 000
05056139245756 K231172 000
05056139245763 K231172 000
05056139246784 K231172 000
05056139246036 K231172 000
05056139246029 K231172 000
05056139246012 K231172 000
05056139246005 K231172 000
05056139245862 K231172 000
05056139245831 K231172 000
05056139245824 K231172 000
05056139244919 K231172 000

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