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510(k) FDA Premarket Notification K241135

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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
00850057117141 K241135 000
00850057117134 K241135 000
00850057117127 K241135 000
00850057117363 K241135 000
00850057117103 K241135 000
00850057117097 K241135 000
00850057117356 K241135 000
00850057117073 K241135 000
00850057117066 K241135 000
00850057117349 K241135 000
00850057117042 K241135 000
00850057117035 K241135 000
00850057117028 K241135 000
00850057117011 K241135 000
00850057117158 K241135 000
00850057117165 K241135 000
00850057117295 K241135 000
00850057117288 K241135 000
00850057117271 K241135 000
00850057117264 K241135 000
00850057117257 K241135 000
00850057117240 K241135 000
00850057117233 K241135 000
00850057117226 K241135 000
00850057117219 K241135 000
00850057117318 K241135 000
00850057117325 K241135 000
00850057117301 K241135 000
00850057117332 K241135 000
00850057117004 K241135 000

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Filename: fda.report/pmn_item.php

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Function: _error_handler

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