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510(k) FDA Premarket Notification K242042

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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
10705034599977 K242042 000
10705034599960 K242042 000
10705034596877 K242042 000
10705034596860 K242042 000
10705034596853 K242042 000

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