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510(k) FDA Premarket Notification K210214

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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
00195377056351 K210214 000
00195377055927 K210214 000
00195377053190 K210214 000
00195377053183 K210214 000
00195377053176 K210214 000
00195377053169 K210214 000
00195377053152 K210214 000
00195377053145 K210214 000
00195377053138 K210214 000
00195377053121 K210214 000
00195377053114 K210214 000
00195377039644 K210214 000
00195377039637 K210214 000
00195377163615 K210214 000
00195377055934 K210214 000
00195377055972 K210214 000
00195377056306 K210214 000
00195377056443 K210214 000
00195377056436 K210214 000
00195377056429 K210214 000
00195377056412 K210214 000
00195377056405 K210214 000
00195377056399 K210214 000
00195377056382 K210214 000
00195377056375 K210214 000
00195377056368 K210214 000
00195377056344 K210214 000
00195377056337 K210214 000
00195377056320 K210214 000
00195377056313 K210214 000
00195377162175 K210214 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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