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510(k) FDA Premarket Notification K240613

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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
07630894812224 K240613 000
07630894812385 K240613 000
07630894812392 K240613 000
07630894812422 K240613 000
07630894812439 K240613 000
07630894812446 K240613 000
07630894812453 K240613 000
07630894812460 K240613 000
07630894812477 K240613 000
07630894812484 K240613 000
07630894812491 K240613 000
07630894812507 K240613 000
07630894812514 K240613 000
07630894812378 K240613 000
07630894812361 K240613 000
07630894812354 K240613 000
07630894812231 K240613 000
07630894812248 K240613 000
07630894812255 K240613 000
07630894812262 K240613 000
07630894812279 K240613 000
07630894812286 K240613 000
07630894812293 K240613 000
07630894812309 K240613 000
07630894812316 K240613 000
07630894812323 K240613 000
07630894812330 K240613 000
07630894812347 K240613 000
07630894812521 K240613 000
07630894812538 K240613 000
07630894812699 K240613 000
07630894812705 K240613 000
07630894812712 K240613 000
07630894812729 K240613 000
07630894812736 K240613 000
07630894812743 K240613 000
07630894812750 K240613 000
07630894812767 K240613 000
07630894812774 K240613 000
07630894812781 K240613 000
07630894812798 K240613 000
07630894812804 K240613 000
07630894812682 K240613 000
07630894812675 K240613 000
07630894812668 K240613 000
07630894812545 K240613 000
07630894812552 K240613 000
07630894812569 K240613 000
07630894812576 K240613 000
07630894812583 K240613 000
07630894812590 K240613 000
07630894812606 K240613 000
07630894812613 K240613 000
07630894812620 K240613 000
07630894812637 K240613 000
07630894812644 K240613 000
07630894812651 K240613 000
07630894812811 K240613 000

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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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