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510(k) FDA Premarket Notification K250452

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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
16975339628120 K250452 000
16975339628274 K250452 000
16975339628281 K250452 000
16975339628298 K250452 000
16975339628304 K250452 000
16975339628311 K250452 000
16975339628328 K250452 000
16975339628335 K250452 000
16975339628342 K250452 000
16975339628359 K250452 000
16975339628366 K250452 000
16975339628373 K250452 000
16975339628380 K250452 000
16975339628267 K250452 000
16975339628250 K250452 000
16975339628137 K250452 000
16975339628144 K250452 000
16975339628151 K250452 000
16975339628168 K250452 000
16975339628175 K250452 000
16975339628182 K250452 000
16975339628199 K250452 000
16975339628205 K250452 000
16975339628212 K250452 000
16975339628229 K250452 000
16975339628236 K250452 000
16975339628243 K250452 000
16975339628397 K250452 000
16975339627567 K250452 000
16975339627710 K250452 000
16975339627727 K250452 000
16975339627734 K250452 000
16975339627741 K250452 000
16975339627758 K250452 000
16975339627765 K250452 000
16975339627772 K250452 000
16975339627789 K250452 000
16975339627796 K250452 000
16975339627802 K250452 000
16975339627819 K250452 000
16975339627826 K250452 000
16975339627703 K250452 000
16975339627697 K250452 000
16975339627574 K250452 000
16975339627581 K250452 000
16975339627598 K250452 000
16975339627604 K250452 000
16975339627611 K250452 000
16975339627628 K250452 000
16975339627635 K250452 000
16975339627642 K250452 000
16975339627659 K250452 000
16975339627666 K250452 000
16975339627673 K250452 000
16975339627680 K250452 000
16975339627833 K250452 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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