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FDA 510(k)

Vessel Sealer Curved (480522)

K-Number: K250674 · 2025-06-13

ApplicantIntuitive Surgical, Inc.
Decision Date2025-06-13
Product CodeNAY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Vessel Sealer Curved (480522) is a medical device manufactured by Intuitive Surgical, Inc.. It received FDA 510(k) clearance on 2025-06-13 under approval number K250674. 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 Vessel Sealer Curved (480522)?

Vessel Sealer Curved (480522) is a medical device that received FDA 510(k) clearance on 2025-06-13. It is manufactured by Intuitive Surgical, Inc.. The 510(k) number is K250674.

When was Vessel Sealer Curved (480522) approved by the FDA?

Vessel Sealer Curved (480522) received FDA 510(k) clearance on 2025-06-13, under approval number K250674.

What company makes Vessel Sealer Curved (480522)?

Vessel Sealer Curved (480522) is manufactured by Intuitive Surgical, Inc..

What is the FDA product code for Vessel Sealer Curved (480522)?

The FDA product code for Vessel Sealer Curved (480522) is NAY.

Other Devices by Intuitive Surgical, Inc.

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Related Devices (Code: NAY)

K162411da Vinci Xi 12 – 8 mm ReducerIntuitive Surgical, Inc. K153276da Vinci Xi Surgical SystemIntuitive Surgical, Inc. K161271da Vinci Xi Surgical SystemIntuitive Surgical, Inc. K152892da Vinci Xi Surgical SystemIntuitive Surgical K152578da Vinci Surgical System, Model IS4000Intuitive Surgical, Inc. K152448da Vinci Single-Site Instrument and AccessoriesIntuitive Surgical, Inc.

Official Source

View on FDA Database →

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

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