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510(k) FDA Premarket Notification K220706

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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
07630971287624 K220706 000
07630971292536 K220706 000
07630971287518 K220706 000
07630971287525 K220706 000
07630971287532 K220706 000
07630971287549 K220706 000
07630971287556 K220706 000
07630971287563 K220706 000
07630971287570 K220706 000
07630971287587 K220706 000
07630971287594 K220706 000
07630971287600 K220706 000
07630971287617 K220706 000
07630971292529 K220706 000

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