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510(k) FDA Premarket Notification K230064

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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
07290115753141 K230064 000
07290115752632 K230064 000
07290115752625 K230064 000
07290115752618 K230064 000
07290115752601 K230064 000
07290115752120 K230064 000
07290115752816 K230064 000
07290115752458 K230064 000
07290115752441 K230064 000
07290115752694 K230064 000
07290115752687 K230064 000
07290115752670 K230064 000
07290115752663 K230064 000
07290115752649 K230064 000
07290115752656 K230064 000
07290115752717 K230064 000
07290115752861 K230064 000
07290115752854 K230064 000
07290115752847 K230064 000
07290115752830 K230064 000
07290115752823 K230064 000
07290115752809 K230064 000
07290115752793 K230064 000
07290115752779 K230064 000
07290115751437 K230064 000
07290115752748 K230064 000
07290115752731 K230064 000
07290115752724 K230064 000
07290115752076 K230064 000

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Filename: fda.report/pmn_item.php

Line Number: 156

Backtrace:

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Line: 156
Function: _error_handler

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