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510(k) FDA Premarket Notification K231127

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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
07899995278050 K231127 000
07899995244901 K231127 000
07899995244895 K231127 000
07899995244888 K231127 000
07899995244871 K231127 000
07899995244864 K231127 000
07899995244857 K231127 000
07899995244840 K231127 000
07899995244833 K231127 000
07899995244826 K231127 000
07899995244819 K231127 000
07899995244802 K231127 000
07899995244796 K231127 000
07899995263483 K231127 000
07899995262479 K231127 000
07899995244918 K231127 000
07899995262622 K231127 000
07899995262653 K231127 000
07899995278036 K231127 000
07899995277527 K231127 000
07899995274380 K231127 000
07899995272140 K231127 000
07899995262943 K231127 000
07899995262936 K231127 000
07899995262912 K231127 000
07899995262899 K231127 000
07899995262882 K231127 000
07899995262820 K231127 000
07899995262783 K231127 000
07899995262769 K231127 000
07899995262752 K231127 000
07899995262721 K231127 000
07899995262462 K231127 000

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Filename: fda.report/pmn_item.php

Line Number: 156

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Function: _error_handler

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