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510(k) FDA Premarket Notification K243670

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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
03700780601622 K243670 000
03700780601745 K243670 000
03700780601752 K243670 000
03700780601769 K243670 000
03700780601776 K243670 000
03700780601783 K243670 000
03700780601790 K243670 000
03700780601806 K243670 000
03700780601813 K243670 000
03700780601820 K243670 000
03700780601738 K243670 000
03700780601721 K243670 000
03700780601639 K243670 000
03700780601646 K243670 000
03700780601653 K243670 000
03700780601660 K243670 000
03700780601677 K243670 000
03700780601684 K243670 000
03700780601691 K243670 000
03700780601707 K243670 000
03700780601714 K243670 000
03700780601837 K243670 000
03700780601844 K243670 000
03700780601851 K243670 000
03700780613427 K243670 000
03700780613434 K243670 000
03700780613441 K243670 000
03700780613458 K243670 000
03700780613465 K243670 000
03700780613472 K243670 000
03700780613489 K243670 000
03700780613496 K243670 000
03700780613502 K243670 000
03700780602803 K243670 000
03700780602797 K243670 000
03700780601868 K243670 000
03700780601875 K243670 000
03700780601882 K243670 000
03700780602735 K243670 000
03700780602742 K243670 000
03700780602759 K243670 000
03700780602766 K243670 000
03700780602773 K243670 000
03700780602780 K243670 000
03700780613519 K243670 000

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Filename: fda.report/pmn_item.php

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Line: 156
Function: _error_handler


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