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510(k) FDA Premarket Notification K232220

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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
08809892369842 K232220 000
08809892367336 K232220 000
08809892367312 K232220 000
08809892367305 K232220 000
08809892367244 K232220 000
08809892367206 K232220 000
08809892367138 K232220 000
08809892367121 K232220 000
08809892367060 K232220 000
08809892367046 K232220 000
08809892367039 K232220 000
08809892366988 K232220 000
08809892366964 K232220 000
08809892366957 K232220 000
08809892366896 K232220 000
08809892367381 K232220 000
08809892367398 K232220 000
08809892369835 K232220 000
08809892369828 K232220 000
08809892369347 K232220 000
08809892369330 K232220 000
08809892369323 K232220 000
08809892369316 K232220 000
08809892367688 K232220 000
08809892367671 K232220 000
08809892367572 K232220 000
08809892367565 K232220 000
08809892367558 K232220 000
08809892367480 K232220 000
08809892367473 K232220 000
08809892367411 K232220 000
08809892366858 K232220 000

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Filename: fda.report/pmn_item.php

Line Number: 156

Backtrace:

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Line: 156
Function: _error_handler


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