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510(k) FDA Premarket Notification K230705

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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
06958481438321 K230705 000
06958481438451 K230705 000
06958481438468 K230705 000
06958481438475 K230705 000
06958481438482 K230705 000
06958481438499 K230705 000
06958481438505 K230705 000
06958481438512 K230705 000
06958481438529 K230705 000
06958481438536 K230705 000
06958481438543 K230705 000
06958481438444 K230705 000
06958481438437 K230705 000
06958481438338 K230705 000
06958481438345 K230705 000
06958481438352 K230705 000
06958481438369 K230705 000
06958481438376 K230705 000
06958481438383 K230705 000
06958481438390 K230705 000
06958481438406 K230705 000
06958481438413 K230705 000
06958481438420 K230705 000
06958481438550 K230705 000
06958481438567 K230705 000
06958481438574 K230705 000
06958481438703 K230705 000
06958481438710 K230705 000
06958481438727 K230705 000
06958481438734 K230705 000
06958481438741 K230705 000
06958481438758 K230705 000
06958481438765 K230705 000
06958481438772 K230705 000
06958481438789 K230705 000
06958481438796 K230705 000
06958481438697 K230705 000
06958481438680 K230705 000
06958481438581 K230705 000
06958481438598 K230705 000
06958481438604 K230705 000
06958481438611 K230705 000
06958481438628 K230705 000
06958481438635 K230705 000
06958481438642 K230705 000
06958481438659 K230705 000
06958481438666 K230705 000
06958481438673 K230705 000
06958481438802 K230705 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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