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510(k) FDA Premarket Notification K241539

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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
03700569671105 K241539 000
03700569645847 K241539 000
03700569645830 K241539 000
03700569645823 K241539 000
03700569645816 K241539 000
03700569645809 K241539 000
03700569642266 K241539 000
03700569642259 K241539 000
03700569642242 K241539 000
03700569642235 K241539 000
03700569642228 K241539 000
03700569642211 K241539 000
03700569645854 K241539 000
03700569645861 K241539 000
03700569671099 K241539 000
03700569671082 K241539 000
03700569671075 K241539 000
03700569645953 K241539 000
03700569645946 K241539 000
03700569645939 K241539 000
03700569645922 K241539 000
03700569645915 K241539 000
03700569645908 K241539 000
03700569645885 K241539 000
03700569645878 K241539 000
03700569642204 K241539 000

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Filename: fda.report/pmn_item.php

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Line: 156
Function: _error_handler

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