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510(k) FDA Premarket Notification K243530

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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
08435673502599 K243530 000
08436568733197 K243530 000
08436568733340 K243530 000
08436568733517 K243530 000
08436568734262 K243530 000
08436568734279 K243530 000
08436568734620 K243530 000
08436568735009 K243530 000
08436568735115 K243530 000
08436568735269 K243530 000
08436568735870 K243530 000
08436568733098 K243530 000
08436568733081 K243530 000
08435673502698 K243530 000
08435673505590 K243530 000
08435673505606 K243530 000
08435673505613 K243530 000
08435673505620 K243530 000
08436568730417 K243530 000
08436568730424 K243530 000
08436568730431 K243530 000
08436568730448 K243530 000
08436568732978 K243530 000
08436568735993 K243530 000
08436568736167 K243530 000
08436568736174 K243530 000
08436568737294 K243530 000
08436568737300 K243530 000
08436568737317 K243530 000
08436568738239 K243530 000
08436568738246 K243530 000
08436568738253 K243530 000
08436568730554 K243530 000
08436568731032 K243530 000
08436568731063 K243530 000
08436568731513 K243530 000
08436568737287 K243530 000
08436568737188 K243530 000
08436568736235 K243530 000
08436568737096 K243530 000
08436568737102 K243530 000
08436568737119 K243530 000
08436568737126 K243530 000
08436568737133 K243530 000
08436568737140 K243530 000
08436568737157 K243530 000
08436568737164 K243530 000
08436568737171 K243530 000
08436568731636 K243530 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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