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510(k) FDA Premarket Notification K152836

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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
07332747111712 K152836 000
07332747161663 K152836 000
07332747102857 K152836 000
07332747102871 K152836 000
07332747105155 K152836 000
07332747105162 K152836 000
07332747105179 K152836 000
07332747105186 K152836 000
07332747105193 K152836 000
07332747105216 K152836 000
07332747105254 K152836 000
07332747105322 K152836 000
07332747111651 K152836 000
07332747111668 K152836 000
07332747111675 K152836 000
07332747111682 K152836 000
07332747111705 K152836 000
07332747161649 K152836 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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