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FDA 510(k)

da Vinci Surgical System (IS5000)

K-Number: K241284 · 2024-07-03

Decision Date2024-07-03
Product CodeNAY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

da Vinci Surgical System (IS5000) is a medical device manufactured by Intuitive Surgical, Inc.. It received FDA 510(k) clearance on 2024-07-03 under approval number K241284. 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 Surgical System (IS5000)?

da Vinci Surgical System (IS5000) is a medical device that received FDA 510(k) clearance on 2024-07-03. It is manufactured by Intuitive Surgical, Inc.. The 510(k) number is K241284.

When was da Vinci Surgical System (IS5000) approved by the FDA?

da Vinci Surgical System (IS5000) received FDA 510(k) clearance on 2024-07-03, under approval number K241284.

What company makes da Vinci Surgical System (IS5000)?

da Vinci Surgical System (IS5000) is manufactured by Intuitive Surgical, Inc..

What is the FDA product code for da Vinci Surgical System (IS5000)?

The FDA product code for da Vinci Surgical System (IS5000) is NAY.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.