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510(k) FDA Premarket Notification K231413

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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
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08435566630026 K231413 000
08435566630019 K231413 000
08435566628528 K231413 000
08435566628511 K231413 000
08435566626968 K231413 000
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08435566603440 K231413 000

A PHP Error was encountered

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Filename: fda.report/pmn_item.php

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Backtrace:

File: /var/www/fda.report/pmn_item.php
Line: 156
Function: _error_handler


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