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510(k) FDA Premarket Notification P020002

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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
15420045508163 P020002 000
15420045500990 P020002 000
15420045501034 P020002 000
15420045501041 P020002 000
15420045504097 P020002 000
15420045504035 P020002 000
15420045504042 P020002 000
15420045504080 P020002 000
15420045504103 P020002 000
15420045507258 P020002 000
15420045500983 P020002 000
15420045500976 P020002 000
15420045500945 P020002 000
15420045508156 P020002 000
15420045507265 P020002 000
15420045500921 P020002 000
15420045515062 P020002 000
15420045500914 P020002 000
15420045500938 P020002 000
15420045515062 P020002 006
15420045504097 P020002 007
15420045500976 P020002 007
15420045508156 P020002 007
15420045508163 P020002 007
15420045500891 P020002 007
15420045504103 P020002 007
15420045504080 P020002 007
15420045504042 P020002 007
15420045504035 P020002 007
15420045501041 P020002 007
15420045501034 P020002 007
15420045501027 P020002 007
15420045501010 P020002 007
15420045501003 P020002 007
15420045500907 P020002 007
15420045500914 P020002 007
15420045500921 P020002 007
15420045500938 P020002 007
15420045500945 P020002 007
15420045500983 P020002 007
15420045500990 P020002 007
15420045507258 P020002 010
15420045507265 P020002 010

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Function: _error_handler

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