Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

EndoWrist Mercury Bipolar Grasper

K-Number: K180351 · 2018-08-07

ApplicantIntuitive Surgical, Inc.
Decision Date2018-08-07
Product CodeNAY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EndoWrist Mercury Bipolar Grasper is a medical device manufactured by Intuitive Surgical, Inc.. It received FDA 510(k) clearance on 2018-08-07 under approval number K180351. 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 EndoWrist Mercury Bipolar Grasper?

EndoWrist Mercury Bipolar Grasper is a medical device that received FDA 510(k) clearance on 2018-08-07. It is manufactured by Intuitive Surgical, Inc.. The 510(k) number is K180351.

When was EndoWrist Mercury Bipolar Grasper approved by the FDA?

EndoWrist Mercury Bipolar Grasper received FDA 510(k) clearance on 2018-08-07, under approval number K180351.

What company makes EndoWrist Mercury Bipolar Grasper?

EndoWrist Mercury Bipolar Grasper is manufactured by Intuitive Surgical, Inc..

What is the FDA product code for EndoWrist Mercury Bipolar Grasper?

The FDA product code for EndoWrist Mercury Bipolar Grasper is NAY.

Other Devices by Intuitive Surgical, Inc.

K162411da Vinci Xi 12 – 8 mm Reducer K153276da Vinci Xi Surgical System K161271da Vinci Xi Surgical System K152578da Vinci Surgical System, Model IS4000 K152448da Vinci Single-Site Instrument and Accessories K152421IS4000 Stapler 30 Instrument and Stapler 30 Reloads

View all 107 devices →

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.

↑