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INTUITIVE SURGICAL STERO VIEW ENDOSCOPIC SYSTEM

K013952 Class II Traditional
Decision Date
2002-02-28
Sponsor / Applicant
Intuitive Surgical, Inc.

Technical Specification

510(k) Submission ID K013952
Product Code GCJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2002-02-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INTUITIVE SURGICAL STERO VIEW ENDOSCOPIC SYSTEM received FDA 510(k) clearance under submission number K013952, sponsored by Intuitive Surgical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2002-02-28.

Classification & Regulation

This clearance is catalogued under FDA product code GCJ and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.