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510(k) FDA Premarket Notification K230537

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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
00810094700942 K230537 000
00810094700805 K230537 000
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00810094700171 K230537 000
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00810094700140 K230537 000
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00810094700331 K230537 000
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00810094700300 K230537 000
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00810094700270 K230537 000
00810094700133 K230537 000
00810094700959 K230537 000
00814703019654 K230537 000
00814703019517 K230537 000
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00814703019494 K230537 000
00814703019487 K230537 000
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00814703019456 K230537 000
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00814703019432 K230537 000
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00814703019647 K230537 000
00814703019630 K230537 000
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00814703019609 K230537 000
00814703019593 K230537 000
00814703019586 K230537 000
00814703019579 K230537 000
00814703019562 K230537 000
00814703019555 K230537 000
00814703019418 K230537 000
00814703019401 K230537 000
00814703019395 K230537 000
00810094700430 K230537 000
00810094700423 K230537 000
00810094700416 K230537 000
00814703019999 K230537 000
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00814703019388 K230537 000
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00814703019364 K230537 000
00814703019357 K230537 000
00814703019340 K230537 000
00814703019333 K230537 000
00814703019326 K230537 000
00814703019319 K230537 000
00814703019302 K230537 000
00814703019296 K230537 000
00810094700966 K230537 000

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Backtrace:

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


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