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510(k) FDA Premarket Notification K251089

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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
10020221663928 K251089 000
10020221264255 K251089 000
10020221264156 K251089 000
10020221264132 K251089 000
10020221264019 K251089 000
20020221262661 K251089 000
20020221262319 K251089 000
20020221262012 K251089 000
00020221261066 K251089 000
10020221260677 K251089 000
10020221260660 K251089 000
10020221260516 K251089 000
20020221260483 K251089 000
10020221264309 K251089 000
10020221264361 K251089 000
20020221271120 K251089 000
20020221271113 K251089 000
20020221271106 K251089 000
20020221271083 K251089 000
20020221271076 K251089 000
20020221271052 K251089 000
20020221271045 K251089 000
20020221271021 K251089 000
20020221271014 K251089 000
20020221271007 K251089 000
20020221270444 K251089 000
10020221264606 K251089 000
10020221260455 K251089 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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