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510(k) FDA Premarket Notification P060002

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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
04049519009032 P060002 000
04049519008868 P060002 000
04049519008851 P060002 000
04049519008844 P060002 000
04049519008837 P060002 000
04049519008820 P060002 000
04049519008813 P060002 000
04049519008806 P060002 000
04049519008790 P060002 000
04049519008783 P060002 000
04049519008776 P060002 000
04049519008769 P060002 000
04049519008752 P060002 000
04049519008745 P060002 000
04049519008875 P060002 000
04049519008899 P060002 000
04049519009025 P060002 000
04049519009018 P060002 000
04049519009001 P060002 000
04049519008998 P060002 000
04049519008981 P060002 000
04049519008974 P060002 000
04049519008967 P060002 000
04049519008950 P060002 000
04049519008943 P060002 000
04049519008936 P060002 000
04049519008929 P060002 000
04049519008912 P060002 000
04049519008905 P060002 000
04049519008738 P060002 000

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Filename: fda.report/pmn_item.php

Line Number: 156

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Line: 156
Function: _error_handler


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