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510(k) FDA Premarket Notification K240143

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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
08056591012634 K240143 000
08055510176877 K240143 000
08055510176860 K240143 000
08055510176853 K240143 000
08055510176846 K240143 000
08055510176839 K240143 000
08055510176822 K240143 000
08055510176815 K240143 000
08055510176808 K240143 000
08055510176792 K240143 000
08055510175085 K240143 000
08055510175078 K240143 000
08056591011286 K240143 000
08056591012511 K240143 000
08056591012627 K240143 000
08056591012610 K240143 000
08056591012603 K240143 000
08056591012597 K240143 000
08056591012580 K240143 000
08056591012573 K240143 000
08056591012566 K240143 000
08056591012559 K240143 000
08056591012542 K240143 000
08056591012535 K240143 000
08056591012528 K240143 000
08055510175061 K240143 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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