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510(k) FDA Premarket Notification K192481

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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
08800061643770 K192481 000
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08800061643336 K192481 000
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08800061644012 K192481 000
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08800061643961 K192481 000
08800061643954 K192481 000
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08800061643930 K192481 000
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08800061643794 K192481 000

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Function: _error_handler


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