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510(k) FDA Premarket Notification P020016

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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
00841036081898 P020016 006
00841036060428 P020016 006
00841036060398 P020016 006
00841036060343 P020016 006
00841036060329 P020016 006
00841036036621 P020016 006
00841036036607 P020016 006
00841036036584 P020016 006
00841036036560 P020016 006
00841036036546 P020016 006
00841036036522 P020016 006
00841036036508 P020016 006
00841036036454 P020016 006
00841036036430 P020016 006
00841036011895 P020016 006
00841036011871 P020016 006
00841036063580 P020016 006
00841036064884 P020016 006
00841036081881 P020016 006
00841036081874 P020016 006
00841036081867 P020016 006
00841036081805 P020016 006
00841036081799 P020016 006
00841036081782 P020016 006
00841036081744 P020016 006
00841036081737 P020016 006
00841036081720 P020016 006
00841036081713 P020016 006
00841036081560 P020016 006
00841036081553 P020016 006
00841036081386 P020016 006
00841036081348 P020016 006
00841036075118 P020016 006
00841036011857 P020016 006

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Filename: fda.report/pmn_item.php

Line Number: 156

Backtrace:

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Line: 156
Function: _error_handler

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