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FDA 510(k)

da Vinci Firefly Imaging System

K-Number: K222827 · 2022-10-20

Decision Date2022-10-20
Product CodeNAY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

da Vinci Firefly Imaging System is a medical device manufactured by Intuitive Surgical, Inc.. It received FDA 510(k) clearance on 2022-10-20 under approval number K222827. The device is classified under product code NAY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the da Vinci Firefly Imaging System?

da Vinci Firefly Imaging System is a medical device that received FDA 510(k) clearance on 2022-10-20. It is manufactured by Intuitive Surgical, Inc.. The 510(k) number is K222827.

When was da Vinci Firefly Imaging System approved by the FDA?

da Vinci Firefly Imaging System received FDA 510(k) clearance on 2022-10-20, under approval number K222827.

What company makes da Vinci Firefly Imaging System?

da Vinci Firefly Imaging System is manufactured by Intuitive Surgical, Inc..

What is the FDA product code for da Vinci Firefly Imaging System?

The FDA product code for da Vinci Firefly Imaging System is NAY.

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Official Source

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