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510(k) FDA Premarket Notification K250163

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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
07613327649109 K250163 000
07613327649383 K250163 000
07613327649390 K250163 000
07613327649406 K250163 000
07613327649413 K250163 000
07613327649420 K250163 000
07613327649437 K250163 000
07613327649444 K250163 000
07613327649451 K250163 000
07613327649468 K250163 000
07613327649475 K250163 000
07613327649482 K250163 000
07613327649499 K250163 000
07613327649376 K250163 000
07613327649369 K250163 000
07613327649130 K250163 000
07613327649253 K250163 000
07613327649260 K250163 000
07613327649277 K250163 000
07613327649284 K250163 000
07613327649291 K250163 000
07613327649307 K250163 000
07613327649314 K250163 000
07613327649321 K250163 000
07613327649338 K250163 000
07613327649345 K250163 000
07613327649352 K250163 000
07613327649505 K250163 000
07613327649512 K250163 000
07613327649529 K250163 000
07613327649673 K250163 000
07613327649697 K250163 000
07613327649703 K250163 000
07613327649727 K250163 000
07613327649734 K250163 000
07613327649741 K250163 000
07613327649758 K250163 000
07613327649772 K250163 000
07613327649789 K250163 000
07613327649796 K250163 000
07613327649802 K250163 000
07613327659436 K250163 000
07613327649666 K250163 000
07613327649659 K250163 000
07613327649536 K250163 000
07613327649543 K250163 000
07613327649550 K250163 000
07613327649567 K250163 000
07613327649574 K250163 000
07613327649581 K250163 000
07613327649598 K250163 000
07613327649604 K250163 000
07613327649611 K250163 000
07613327649628 K250163 000
07613327649635 K250163 000
07613327649642 K250163 000
07613327659443 K250163 000

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Severity: Notice

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Filename: fda.report/pmn_item.php

Line Number: 156

Backtrace:

File: /var/www/fda.report/pmn_item.php
Line: 156
Function: _error_handler


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