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510(k) FDA Premarket Notification K231844

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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
07290014381032 K231844 000
07290115933734 K231844 000
07290115933741 K231844 000
07290115933758 K231844 000
07290115933765 K231844 000
07290115933772 K231844 000
07290115933789 K231844 000
07290115933796 K231844 000
07290115933802 K231844 000
07290115933819 K231844 000
07290115933826 K231844 000
07290115933833 K231844 000
07290115933840 K231844 000
07290115933857 K231844 000
07290115933727 K231844 000
07290115933659 K231844 000
07290014381049 K231844 000
07290014381056 K231844 000
07290115933246 K231844 000
07290115933253 K231844 000
07290115933260 K231844 000
07290115933277 K231844 000
07290115933284 K231844 000
07290115933291 K231844 000
07290115933604 K231844 000
07290115933611 K231844 000
07290115933628 K231844 000
07290115933635 K231844 000
07290115933642 K231844 000
07290115933864 K231844 000
07290115933871 K231844 000
07290115931914 K231844 000
07290115931921 K231844 000
07290115931938 K231844 000
07290115931945 K231844 000
07290115931952 K231844 000
07290115931969 K231844 000
07290115931976 K231844 000
07290115931983 K231844 000
07290115931990 K231844 000
07290115932003 K231844 000
07290115932010 K231844 000
07290115933697 K231844 000
07290115933703 K231844 000
07290115931907 K231844 000
07290115931891 K231844 000
07290115933888 K231844 000
07290115933895 K231844 000
07290115933901 K231844 000
07290115933918 K231844 000
07290115933925 K231844 000
07290115931815 K231844 000
07290115931822 K231844 000
07290115931839 K231844 000
07290115931846 K231844 000
07290115931853 K231844 000
07290115931860 K231844 000
07290115931877 K231844 000
07290115931884 K231844 000
07290115933710 K231844 000

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Severity: Notice

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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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