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510(k) FDA Premarket Notification K230002

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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
20847212008431 K230002 000
00840369321770 K230002 000
00840369321800 K230002 000
00840369321718 K230002 000
20847212008486 K230002 000
20847212008493 K230002 000
20847212008509 K230002 000
20847212008516 K230002 000
20847212008400 K230002 000
20847212008417 K230002 000
20847212008424 K230002 000
00840369321749 K230002 000

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