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510(k) FDA Premarket Notification K250830

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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
06976006415138 K250830 000
06976006415022 K250830 000
06976006415039 K250830 000
06976006415046 K250830 000
06976006415053 K250830 000
06976006415060 K250830 000
06976006415077 K250830 000
06976006415084 K250830 000
06976006415091 K250830 000
06976006415107 K250830 000
06976006415114 K250830 000
06976006415121 K250830 000
06976006415015 K250830 000

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