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510(k) FDA Premarket Notification K221572

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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
00840283402081 K221572 000
00840283405839 K221572 000
00840283401725 K221572 000
00840283401954 K221572 000
00840283401961 K221572 000
00840283401978 K221572 000
00840283402005 K221572 000
00840283402012 K221572 000
00840283402036 K221572 000
00840283402043 K221572 000
00840283402050 K221572 000
00840283402067 K221572 000
00840283401664 K221572 000

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