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510(k) FDA Premarket Notification K231314

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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
00688346002485 K231314 000
00688346002638 K231314 000
00688346002645 K231314 000
00688346002669 K231314 000
00688346002676 K231314 000
00688346002683 K231314 000
00688346002690 K231314 000
00688346002706 K231314 000
00688346002713 K231314 000
00688346002720 K231314 000
00688346002737 K231314 000
00688346002744 K231314 000
00688346002621 K231314 000
00688346002614 K231314 000
00688346002607 K231314 000
00688346002492 K231314 000
00688346002508 K231314 000
00688346002515 K231314 000
00688346002522 K231314 000
00688346002539 K231314 000
00688346002546 K231314 000
00688346002553 K231314 000
00688346002560 K231314 000
00688346002577 K231314 000
00688346002584 K231314 000
00688346002591 K231314 000
00688346002751 K231314 000
00688346002768 K231314 000
00688346002775 K231314 000
00688346002928 K231314 000
00688346002935 K231314 000
00688346002942 K231314 000
00688346002959 K231314 000
00688346002966 K231314 000
00688346002973 K231314 000
00688346002980 K231314 000
00688346002997 K231314 000
00688346003000 K231314 000
00688346003017 K231314 000
00688346003024 K231314 000
00688346002911 K231314 000
00688346002904 K231314 000
00688346002898 K231314 000
00688346002782 K231314 000
00688346002799 K231314 000
00688346002805 K231314 000
00688346002812 K231314 000
00688346002829 K231314 000
00688346002836 K231314 000
00688346002843 K231314 000
00688346002850 K231314 000
00688346002867 K231314 000
00688346002874 K231314 000
00688346002881 K231314 000
00688346003031 K231314 000

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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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