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510(k) FDA Premarket Notification K233199

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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
00887868580963 K233199 000
00887868558184 K233199 000
00887868558177 K233199 000
00887868558160 K233199 000
00887868558153 K233199 000
00887868558146 K233199 000
00887868558139 K233199 000
00887868558122 K233199 000
00887868558115 K233199 000
00887868558108 K233199 000
00887868558092 K233199 000
00887868558078 K233199 000
00887868557910 K233199 000
00887868557903 K233199 000
00887868557897 K233199 000
00887868557880 K233199 000
00887868558191 K233199 000
00887868558207 K233199 000
00887868575181 K233199 000
00887868575174 K233199 000
00887868575167 K233199 000
00887868575150 K233199 000
00887868575143 K233199 000
00887868575136 K233199 000
00887868575129 K233199 000
00887868575112 K233199 000
00887868575105 K233199 000
00887868558306 K233199 000
00887868558283 K233199 000
00887868558252 K233199 000
00887868558238 K233199 000
00887868558221 K233199 000
00887868558214 K233199 000
00887868557873 K233199 000

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Message: Undefined index: deviceName

Filename: fda.report/pmn_item.php

Line Number: 156

Backtrace:

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Line: 156
Function: _error_handler

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