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510(k) FDA Premarket Notification K240531

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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
00847236026875 K240531 000
00847236026578 K240531 000
00847236026585 K240531 000
00847236026592 K240531 000
00847236026608 K240531 000
00847236026615 K240531 000
00847236026622 K240531 000
00847236026639 K240531 000
00847236026646 K240531 000
00847236026981 K240531 000
00847236026974 K240531 000
00847236026967 K240531 000
00847236026882 K240531 000
00847236026899 K240531 000
00847236026905 K240531 000
00847236026912 K240531 000
00847236026929 K240531 000
00847236026936 K240531 000
00847236026943 K240531 000
00847236026950 K240531 000
00847236026653 K240531 000
00847236026660 K240531 000
00847236026783 K240531 000
00847236026790 K240531 000
00847236026806 K240531 000
00847236026813 K240531 000
00847236026820 K240531 000
00847236026837 K240531 000
00847236026844 K240531 000
00847236026851 K240531 000
00847236026776 K240531 000
00847236026769 K240531 000
00847236026752 K240531 000
00847236026677 K240531 000
00847236026684 K240531 000
00847236026691 K240531 000
00847236026707 K240531 000
00847236026714 K240531 000
00847236026721 K240531 000
00847236026738 K240531 000
00847236026745 K240531 000
00847236026868 K240531 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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