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510(k) FDA Premarket Notification K242042

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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
10705034584164 K242042 000
10705034596006 K242042 000
10705034596013 K242042 000
10705034596020 K242042 000
10705034596099 K242042 000
10705034596143 K242042 000
10705034596150 K242042 000
10705034596822 K242042 000
10705034596839 K242042 000
10705034596846 K242042 000
10705034599939 K242042 000
10705034599946 K242042 000
10705034599953 K242042 000
10705034595993 K242042 000
10705034595986 K242042 000
10705034595979 K242042 000
10705034584171 K242042 000
10705034587240 K242042 000
10705034587257 K242042 000
10705034587561 K242042 000
10705034587578 K242042 000
10705034587660 K242042 000
10705034587684 K242042 000
10705034587691 K242042 000
10705034587943 K242042 000
10705034587950 K242042 000
10705034587967 K242042 000
10705034587974 K242042 000
10705034600048 K242042 000
10705034600055 K242042 000
10705034601410 K242042 000
10705034601427 K242042 000
10705034601434 K242042 000
10705034645728 K242042 000
10705034645735 K242042 000
10705034645742 K242042 000
10705034645759 K242042 000
10705034645766 K242042 000
10705034596853 K242042 000
10705034596860 K242042 000
10705034596877 K242042 000
10705034599960 K242042 000
10705034601403 K242042 000
10705034601397 K242042 000
10705034601373 K242042 000
10705034600062 K242042 000
10705034600079 K242042 000
10705034600086 K242042 000
10705034600093 K242042 000
10705034600109 K242042 000
10705034600116 K242042 000
10705034600123 K242042 000
10705034601243 K242042 000
10705034601250 K242042 000
10705034601267 K242042 000
10705034601274 K242042 000
10705034601359 K242042 000
10705034599977 K242042 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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