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510(k) FDA Premarket Notification K250197

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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
08059386742518 K250197 000
08059386742662 K250197 000
08059386742679 K250197 000
08059386742686 K250197 000
08059386742693 K250197 000
08059386742709 K250197 000
08059386742716 K250197 000
08059386742723 K250197 000
08059386742730 K250197 000
08059386742747 K250197 000
08059386742754 K250197 000
08059386742761 K250197 000
08059386742655 K250197 000
08059386742648 K250197 000
08059386742631 K250197 000
08059386742525 K250197 000
08059386742532 K250197 000
08059386742549 K250197 000
08059386742556 K250197 000
08059386742563 K250197 000
08059386742570 K250197 000
08059386742587 K250197 000
08059386742594 K250197 000
08059386742600 K250197 000
08059386742617 K250197 000
08059386742624 K250197 000
08059386742778 K250197 000
08059386742785 K250197 000
08059386742938 K250197 000
08059386742945 K250197 000
08059386742952 K250197 000
08059386742969 K250197 000
08059386742976 K250197 000
08059386742983 K250197 000
08059386742990 K250197 000
08059386743003 K250197 000
08059386743010 K250197 000
08059386743027 K250197 000
08059386743034 K250197 000
08059386742921 K250197 000
08059386742914 K250197 000
08059386742907 K250197 000
08059386742792 K250197 000
08059386742808 K250197 000
08059386742815 K250197 000
08059386742822 K250197 000
08059386742839 K250197 000
08059386742846 K250197 000
08059386742853 K250197 000
08059386742860 K250197 000
08059386742877 K250197 000
08059386742884 K250197 000
08059386742891 K250197 000
08059386743041 K250197 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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