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510(k) FDA Premarket Notification K230307

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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
08800053037891 K230307 000
08800053081016 K230307 000
08800053081023 K230307 000
08806169100436 K230307 000
08806169100573 K230307 000
08806169106186 K230307 000
08806169106193 K230307 000
08806169106209 K230307 000
08806169106216 K230307 000
08806169107473 K230307 000
08806169107497 K230307 000
08806169107510 K230307 000
08806169112125 K230307 000
08800053081009 K230307 000
08800053080996 K230307 000
08800053037907 K230307 000
08800053039994 K230307 000
08800053040006 K230307 000
08800053080798 K230307 000
08800053080804 K230307 000
08800053080828 K230307 000
08800053080842 K230307 000
08800053080859 K230307 000
08800053080866 K230307 000
08800053080958 K230307 000
08800053080965 K230307 000
08800053080989 K230307 000
08806169112132 K230307 000
08806169112149 K230307 000
08806169190703 K230307 000
08806169190710 K230307 000
08806169190727 K230307 000
08806169190734 K230307 000
08806169190741 K230307 000
08806169190758 K230307 000
08806169190765 K230307 000
08806169190772 K230307 000
08806169190789 K230307 000
08806169190796 K230307 000
08806169190802 K230307 000
08806169190819 K230307 000
08806169190659 K230307 000
08806169190642 K230307 000
08806169131522 K230307 000
08806169134073 K230307 000
08806169165800 K230307 000
08806169165817 K230307 000
08806169165824 K230307 000
08806169165831 K230307 000
08806169165848 K230307 000
08806169165855 K230307 000
08806169190604 K230307 000
08806169190611 K230307 000
08806169190628 K230307 000
08806169190635 K230307 000
08806169108791 K230307 000

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Filename: fda.report/pmn_item.php

Line Number: 156

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Function: _error_handler


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