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510(k) FDA Premarket Notification K221056

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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
07613365002782 K221056 000
07613365001709 K221056 000
07613365000115 K221056 000
07613365003833 K221056 000
07613365003826 K221056 000
07613365003628 K221056 000
07613365003611 K221056 000
07613365003604 K221056 000
07613365003598 K221056 000
07613365003499 K221056 000
07613365003093 K221056 000
07613365001846 K221056 000
07613365001914 K221056 000
07613365002713 K221056 000
07613365003475 K221056 000
07613365003468 K221056 000
07613365003024 K221056 000
07613365002829 K221056 000
07613365002812 K221056 000
07613365002805 K221056 000
07613365002799 K221056 000
07613365002706 K221056 000
07613365002584 K221056 000
07613365002072 K221056 000

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