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510(k) FDA Premarket Notification K243809

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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
08033390183840 K243809 000
08033390087933 K243809 000
08033390087926 K243809 000
08033390087919 K243809 000
08033390007160 K243809 000
08033390007153 K243809 000
08033390007146 K243809 000
08033390007139 K243809 000
08033390007122 K243809 000
08033390007115 K243809 000
08033390007108 K243809 000
08033390007092 K243809 000
08033390007085 K243809 000
08033390007078 K243809 000
08033390007061 K243809 000
08033390087940 K243809 000
08033390179898 K243809 000
08033390183833 K243809 000
08033390183666 K243809 000
08033390183642 K243809 000
08033390183574 K243809 000
08033390183482 K243809 000
08033390183475 K243809 000
08033390183352 K243809 000
08033390183314 K243809 000
08033390183307 K243809 000
08033390183291 K243809 000
08033390183284 K243809 000
08033390183260 K243809 000
08033390183253 K243809 000
08033390183246 K243809 000
08033390007054 K243809 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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