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510(k) FDA Premarket Notification K210947

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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
07540209955938 K210947 000
07540209955761 K210947 000
07540209955778 K210947 000
07540209955785 K210947 000
07540209955792 K210947 000
07540209955808 K210947 000
07540209955815 K210947 000
07540209955822 K210947 000
07540209955839 K210947 000
07540209955846 K210947 000
07540209955853 K210947 000
07540209955860 K210947 000
07540209955877 K210947 000
07540209955884 K210947 000
07540209955891 K210947 000
07540209955907 K210947 000
07540209955914 K210947 000
07540209955921 K210947 000
07540209955952 K210947 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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