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510(k) FDA Premarket Notification K230725

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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
08800055777788 K230725 000
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08800055777917 K230725 000
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08800055793740 K230725 000
08800055793733 K230725 000
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08800055777801 K230725 000

A PHP Error was encountered

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Filename: fda.report/pmn_item.php

Line Number: 156

Backtrace:

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


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