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510(k) FDA Premarket Notification N12159

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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
30705031468089 N12159 000
20705031002965 N12159 000
20705031002958 N12159 000
30705031468133 N12159 000
30705031468126 N12159 000
30705031468119 N12159 000
30705031468102 N12159 000
30705031468096 N12159 000
20705031003030 N12159 014
20705031003023 N12159 014
20705031003016 N12159 014
20705031002972 N12159 014
20705031002996 N12159 014
10705031002975 N12159 014
20705031003061 N12159 014
20705031003115 N12159 015
20705031003122 N12159 015
20705031003139 N12159 015
20705031063584 N12159 026
20705031063591 N12159 027
20705031063607 N12159 028
20705031063638 N12159 032
20705031063621 N12159 032
20705031063614 N12159 032
20705031005201 N12159 032
20705031005195 N12159 032
20705031005362 N12159 032
20705031005218 N12159 032
20705031005355 N12159 032
20705031237510 N12159 047

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