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510(k) FDA Premarket Notification K230284

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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
00815948029736 K230284 000
00815948029576 K230284 000
00815948029569 K230284 000
00815948029552 K230284 000
00815948029545 K230284 000
00815948029538 K230284 000
00815948029521 K230284 000
00815948029514 K230284 000
00815948029507 K230284 000
00815948024793 K230284 000
00815948029583 K230284 000
00815948029637 K230284 000
00815948029729 K230284 000
00815948029712 K230284 000
00815948029705 K230284 000
00815948029699 K230284 000
00815948029682 K230284 000
00815948029675 K230284 000
00815948029668 K230284 000
00815948029651 K230284 000
00815948029644 K230284 000
00815948024779 K230284 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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