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510(k) FDA Premarket Notification K231504

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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
00841731137890 K231504 000
00841731137708 K231504 000
00841731137692 K231504 000
00841731137685 K231504 000
00841731137678 K231504 000
00841731137661 K231504 000
00841731137654 K231504 000
00841731137647 K231504 000
00841731137630 K231504 000
00841731137623 K231504 000
00841731137616 K231504 000
00841731137609 K231504 000
00841731137593 K231504 000
00841731137586 K231504 000
00841731137579 K231504 000
00841731137562 K231504 000
00841731137555 K231504 000
00841731137715 K231504 000
00841731137722 K231504 000
00841731137883 K231504 000
00841731137876 K231504 000
00841731137869 K231504 000
00841731137852 K231504 000
00841731137845 K231504 000
00841731137838 K231504 000
00841731137821 K231504 000
00841731137814 K231504 000
00841731137807 K231504 000
00841731137791 K231504 000
00841731137784 K231504 000
00841731137777 K231504 000
00841731137760 K231504 000
00841731137753 K231504 000
00841731137746 K231504 000
00841731137739 K231504 000
00841731137548 K231504 000

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Line: 156
Function: _error_handler

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