Intuitive Surgical EndoWrist Vessel Sealer Extend
K-Number: K173337 · 2018-04-26
Device Summary
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. The listed applicant is Intuitive Surgical, Inc.. The 510(k) number is K173337.
When did Intuitive Surgical EndoWrist Vessel Sealer Extend receive FDA 510(k) clearance?
Intuitive Surgical EndoWrist Vessel Sealer Extend received FDA 510(k) clearance on 2018-04-26, under 510(k) number K173337.
Who is the listed applicant for Intuitive Surgical EndoWrist Vessel Sealer Extend?
The FDA 510(k) record lists Intuitive Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.
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.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Intuitive Surgical, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: NAY)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.