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510(k) FDA Premarket Notification K251780

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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
00810055525874 K251780 000
00810055524839 K251780 000
00810055524822 K251780 000
00810055524815 K251780 000
00810055524808 K251780 000
00810055524792 K251780 000
00810055524785 K251780 000
00810055524778 K251780 000
00810055524761 K251780 000
00810055524846 K251780 000
00810055524853 K251780 000
00810055525133 K251780 000
00810055525126 K251780 000
00810055525119 K251780 000
00810055525102 K251780 000
00810055525096 K251780 000
00810055524891 K251780 000
00810055524884 K251780 000
00810055524860 K251780 000
00810055524754 K251780 000

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