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510(k) FDA Premarket Notification K240701

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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
04056481145491 K240701 000
04056481144760 K240701 000
04056481144777 K240701 000
04056481144784 K240701 000
04056481144791 K240701 000
04056481144807 K240701 000
04056481144814 K240701 000
04056481144821 K240701 000
04056481144838 K240701 000
04056481145057 K240701 000
04056481145064 K240701 000
04056481145071 K240701 000
04056481145088 K240701 000
04056481145095 K240701 000
04056481145835 K240701 000
04056481146306 K240701 000
04056481144753 K240701 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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