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510(k) FDA Premarket Notification K240912

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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
06975801800026 K240912 000
06975801800620 K240912 000
06975801800613 K240912 000
06975801801436 K240912 000
06975801801429 K240912 000
06975801801207 K240912 000
06975801801191 K240912 000
06975801801184 K240912 000
06975801801177 K240912 000
06975801801153 K240912 000
06975801807933 K240912 000
06975801807926 K240912 000
06975801807919 K240912 000
06975801807902 K240912 000
06975801807896 K240912 000
06975801800637 K240912 000
06975801800644 K240912 000
06975801800019 K240912 000
06975801801061 K240912 000
06975801801054 K240912 000
06975801801030 K240912 000
06975801801023 K240912 000
06975801801016 K240912 000
06975801800798 K240912 000
06975801800781 K240912 000
06975801800774 K240912 000
06975801800750 K240912 000
06975801800743 K240912 000
06975801800712 K240912 000
06975801800675 K240912 000
06975801800668 K240912 000
06975801807889 K240912 000

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