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510(k) FDA Premarket Notification P080003

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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
15420045508033 P080003 000
15420045510760 P080003 000
15420045510593 P080003 000
15420045510586 P080003 000
15420045510579 P080003 000
15420045510562 P080003 000
15420045510555 P080003 000
15420045510548 P080003 000
15420045510784 P080003 000
15420045510777 P080003 000
15420045510753 P080003 000
15420045510616 P080003 000
15420045512689 P080003 000
15420045512696 P080003 000
15420045512474 P080003 000
15420045508026 P080003 000
15420045508019 P080003 000
15420045507296 P080003 000
15420045507289 P080003 000
15420045507272 P080003 000
15420045510524 P080003 000
15420045500013 P080003 000
15420045510395 P080003 000
15420045512313 P080003 000
15420045511897 P080003 000
15420045510388 P080003 000
15420045500020 P080003 001
15420045508026 P080003 004
15420045512474 P080003 008

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Line: 156
Function: _error_handler


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