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510(k) FDA Premarket Notification K230626

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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
00195278341129 K230626 000
00195278699916 K230626 000
00195278699923 K230626 000
00840682139250 K230626 000
00195278093998 K230626 000
00195278094001 K230626 000
00195278110435 K230626 000
00195278201980 K230626 000
00195278264794 K230626 000
00195278264800 K230626 000
00195278264817 K230626 000
00195278264824 K230626 000
00195278264831 K230626 000
00195278330413 K230626 000
00195278229229 K230626 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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