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510(k) FDA Premarket Notification K242379

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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
08809918249943 K242379 000
08809918255449 K242379 000
08809918255456 K242379 000
08809918255463 K242379 000
08809918255470 K242379 000
08809918255487 K242379 000
08809918255494 K242379 000
08809918255500 K242379 000
08809918255517 K242379 000
08809918255432 K242379 000
08809918255425 K242379 000
08809918255418 K242379 000
08809918255333 K242379 000
08809918255340 K242379 000
08809918255357 K242379 000
08809918255364 K242379 000
08809918255371 K242379 000
08809918255388 K242379 000
08809918255395 K242379 000
08809918255401 K242379 000
08809918255524 K242379 000
08809918255586 K242379 000
08809918255708 K242379 000
08809918255715 K242379 000
08809918255722 K242379 000
08809918255739 K242379 000
08809918255746 K242379 000
08809918255753 K242379 000
08809918255760 K242379 000
08809918255777 K242379 000
08809918255692 K242379 000
08809918255685 K242379 000
08809918255678 K242379 000
08809918255593 K242379 000
08809918255609 K242379 000
08809918255616 K242379 000
08809918255623 K242379 000
08809918255630 K242379 000
08809918255647 K242379 000
08809918255654 K242379 000
08809918255661 K242379 000
08809918255821 K242379 000

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Filename: fda.report/pmn_item.php

Line Number: 156

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Line: 156
Function: _error_handler

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