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510(k) FDA Premarket Notification K230583

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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
07640332471067 K230583 000
07640332471197 K230583 000
07640332471203 K230583 000
07640332471210 K230583 000
07640332471227 K230583 000
07640332471234 K230583 000
07640332471241 K230583 000
07640332471258 K230583 000
07640332471265 K230583 000
07640332471272 K230583 000
07640332471289 K230583 000
07640332471180 K230583 000
07640332471173 K230583 000
07640332471074 K230583 000
07640332471081 K230583 000
07640332471098 K230583 000
07640332471104 K230583 000
07640332471111 K230583 000
07640332471128 K230583 000
07640332471135 K230583 000
07640332471142 K230583 000
07640332471159 K230583 000
07640332471166 K230583 000
07640332471296 K230583 000
07640332471302 K230583 000
07640332471432 K230583 000
07640332471449 K230583 000
07640332471456 K230583 000
07640332471463 K230583 000
07640332471470 K230583 000
07640332471487 K230583 000
07640332471494 K230583 000
07640332471500 K230583 000
07640332471517 K230583 000
07640332471524 K230583 000
07640332471425 K230583 000
07640332471418 K230583 000
07640332471319 K230583 000
07640332471326 K230583 000
07640332471333 K230583 000
07640332471340 K230583 000
07640332471357 K230583 000
07640332471364 K230583 000
07640332471371 K230583 000
07640332471388 K230583 000
07640332471395 K230583 000
07640332471401 K230583 000
07640332471531 K230583 000

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Severity: Notice

Message: Undefined index: deviceName

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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