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510(k) FDA Premarket Notification K242819

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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
08435566637179 K242819 000
08435566630804 K242819 000
08435566630798 K242819 000
08435566603822 K242819 000
08435566603815 K242819 000
08435566603808 K242819 000
08435566603792 K242819 000
08435566603785 K242819 000
08435566603778 K242819 000
08435566603761 K242819 000
08435566603754 K242819 000
08435566601392 K242819 000
08435566601385 K242819 000
08435566630811 K242819 000
08435566630828 K242819 000
08435566630262 K242819 000
08435566630255 K242819 000
08435566630248 K242819 000
08435566601361 K242819 000
08435566601354 K242819 000
08435566632372 K242819 000
08435566630880 K242819 000
08435566630873 K242819 000
08435566630866 K242819 000
08435566630859 K242819 000
08435566630842 K242819 000
08435566630835 K242819 000
08435566601378 K242819 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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