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510(k) FDA Premarket Notification K243382

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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
04049197177368 K243382 000
04049197178846 K243382 000
04049197179768 K243382 000
04049197179775 K243382 000
04049197179782 K243382 000
04049197180757 K243382 000
04049197180818 K243382 000
04049197393379 K243382 000
04049197393386 K243382 000
04049197393409 K243382 000
04049197393454 K243382 000
04049197393485 K243382 000
04049197178839 K243382 000
04049197178822 K243382 000
04049197178747 K243382 000
04049197177467 K243382 000
04049197177580 K243382 000
04049197177801 K243382 000
04049197178082 K243382 000
04049197178150 K243382 000
04049197178167 K243382 000
04049197178501 K243382 000
04049197178563 K243382 000
04049197178570 K243382 000
04049197178723 K243382 000
04049197178730 K243382 000
04049197393508 K243382 000
04049197393782 K243382 000
04049197393812 K243382 000
04049197506281 K243382 000
04049197507387 K243382 000
04049197515399 K243382 000
04049197516976 K243382 000
04049197517041 K243382 000
04049197517058 K243382 000
04049197517065 K243382 000
04049197517089 K243382 000
04049197522762 K243382 000
04049197524964 K243382 000
04049197547147 K243382 000
04049197503730 K243382 000
04049197495417 K243382 000
04049197495394 K243382 000
04049197450416 K243382 000
04049197450423 K243382 000
04049197450430 K243382 000
04049197450485 K243382 000
04049197495288 K243382 000
04049197495295 K243382 000
04049197495332 K243382 000
04049197495349 K243382 000
04049197495356 K243382 000
04049197495363 K243382 000
04049197495370 K243382 000
04049197547161 K243382 000

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Filename: fda.report/pmn_item.php

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Line: 156
Function: _error_handler


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