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510(k) FDA Premarket Notification K240830

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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
10889981303792 K240830 000
10889981303914 K240830 000
10889981303921 K240830 000
10889981303938 K240830 000
10889981303945 K240830 000
10889981303952 K240830 000
10889981303969 K240830 000
10889981303976 K240830 000
10889981303983 K240830 000
10889981303907 K240830 000
10889981303891 K240830 000
10889981303884 K240830 000
10889981303808 K240830 000
10889981303815 K240830 000
10889981303822 K240830 000
10889981303839 K240830 000
10889981303846 K240830 000
10889981303853 K240830 000
10889981303860 K240830 000
10889981303877 K240830 000
10889981303990 K240830 000
10889981304003 K240830 000
10889981304126 K240830 000
10889981304133 K240830 000
10889981304140 K240830 000
10889981304157 K240830 000
10889981304164 K240830 000
10889981304171 K240830 000
10889981304188 K240830 000
10889981304195 K240830 000
10889981304119 K240830 000
10889981304102 K240830 000
10889981304096 K240830 000
10889981304010 K240830 000
10889981304027 K240830 000
10889981304034 K240830 000
10889981304041 K240830 000
10889981304058 K240830 000
10889981304065 K240830 000
10889981304072 K240830 000
10889981304089 K240830 000
10889981304201 K240830 000

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Function: _error_handler

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