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510(k) FDA Premarket Notification P100003

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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
00889095154795 P100003 000
00889095154948 P100003 000
00889095154931 P100003 000
00889095154924 P100003 000
00889095154917 P100003 000
00889095154900 P100003 000
00889095154894 P100003 000
00889095154887 P100003 000
00889095154870 P100003 000
00889095154863 P100003 000
00889095154856 P100003 000
00889095154849 P100003 000
00889095154832 P100003 000
00889095154825 P100003 000
00889095154818 P100003 000
00889095154801 P100003 000
00889095154955 P100003 000
00889095154962 P100003 000
00889095179132 P100003 000
00889095179101 P100003 000
00889095179095 P100003 000
00889095179064 P100003 000
00889095179057 P100003 000
00889095179149 P100003 000
00889095179187 P100003 005
00889095179194 P100003 005
00889095179170 P100003 005
00889095179163 P100003 005
00889095179156 P100003 005
00889095179125 P100003 005
00889095179118 P100003 005
00889095179088 P100003 005
00889095179071 P100003 005
00889095179200 P100003 005

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Filename: fda.report/pmn_item.php

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Function: _error_handler

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