510(k) FDA Premarket Notification K230374

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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 Identifier	submissionNumber	Supplement
06934184010019	K230374	000
06934184002779	K230374	000
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Backtrace:

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Line: 156
Function: _error_handler