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FDA 510(k)

Intuitive Surgical EndoWrist Vessel Sealer Extend

K-Number: K173337 · 2018-04-26

Decision Date2018-04-26
Product CodeNAY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Intuitive Surgical EndoWrist Vessel Sealer Extend is a medical device manufactured by Intuitive Surgical, Inc.. It received FDA 510(k) clearance on 2018-04-26 under approval number K173337. 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 Intuitive Surgical EndoWrist Vessel Sealer Extend?

Intuitive Surgical EndoWrist Vessel Sealer Extend is a medical device that received FDA 510(k) clearance on 2018-04-26. It is manufactured by Intuitive Surgical, Inc.. The 510(k) number is K173337.

When was Intuitive Surgical EndoWrist Vessel Sealer Extend approved by the FDA?

Intuitive Surgical EndoWrist Vessel Sealer Extend received FDA 510(k) clearance on 2018-04-26, under approval number K173337.

What company makes Intuitive Surgical EndoWrist Vessel Sealer Extend?

Intuitive Surgical EndoWrist Vessel Sealer Extend is manufactured by Intuitive Surgical, Inc..

What is the FDA product code for Intuitive Surgical EndoWrist Vessel Sealer Extend?

The FDA product code for Intuitive Surgical EndoWrist Vessel Sealer Extend 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.