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510(k) FDA Premarket Notification K252401

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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
04048844693602 K252401 000
04048844693374 K252401 000
04048844693350 K252401 000
04048844781101 K252401 000
04048844732097 K252401 000
04048844732080 K252401 000
04048844732066 K252401 000
04048844732059 K252401 000
04048844732042 K252401 000
04048844732028 K252401 000
04048844732004 K252401 000
04048844731991 K252401 000
04048844731984 K252401 000
04048844731977 K252401 000
04048844693381 K252401 000
04048844693398 K252401 000
04048844693404 K252401 000
04048844693589 K252401 000
04048844693572 K252401 000
04048844693558 K252401 000
04048844693541 K252401 000
04048844693534 K252401 000
04048844693527 K252401 000
04048844693503 K252401 000
04048844693497 K252401 000
04048844693473 K252401 000
04048844693466 K252401 000
04048844693459 K252401 000
04048844693435 K252401 000
04048844693428 K252401 000
04048844732103 K252401 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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