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510(k) FDA Premarket Notification K233439

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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
06933741402502 K233439 000
06933741401796 K233439 000
06933741401789 K233439 000
06933741401772 K233439 000
06933741401758 K233439 000
06933741401741 K233439 000
06933741401734 K233439 000
06933741401727 K233439 000
06933741401710 K233439 000
06933741401697 K233439 000
06933741401802 K233439 000
06933741401819 K233439 000
06933741402120 K233439 000
06933741402045 K233439 000
06933741402021 K233439 000
06933741401895 K233439 000
06933741401871 K233439 000
06933741401857 K233439 000
06933741401840 K233439 000
06933741401833 K233439 000
06933741401826 K233439 000
06933741401673 K233439 000

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