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510(k) FDA Premarket Notification K053014

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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
00359883006525 K053014 000
00359883001667 K053014 000
00359883001650 K053014 000
00359883001643 K053014 000
00359883001629 K053014 000
00359883001605 K053014 000
00359883001599 K053014 000
00359883001582 K053014 000
00359883001575 K053014 000
00359883001568 K053014 000
00359883001544 K053014 000
00359883001520 K053014 000
00359883001513 K053014 000
00359883001506 K053014 000
00359883001490 K053014 000
00359883001674 K053014 000
00359883001704 K053014 000
00359883006006 K053014 000
00359883005993 K053014 000
00359883005986 K053014 000
00359883002404 K053014 000
00359883002343 K053014 000
00359883002305 K053014 000
00359883002268 K053014 000
00359883002220 K053014 000
00359883002183 K053014 000
00359883002084 K053014 000
00359883002022 K053014 000
00359883001964 K053014 000
00359883001902 K053014 000
00359883001827 K053014 000
00359883001483 K053014 000

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Message: Undefined index: deviceName

Filename: fda.report/pmn_item.php

Line Number: 156

Backtrace:

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Line: 156
Function: _error_handler


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