meddevicedb.com FDA Device Reference

SureForm 45 Curved Tip, SureForm 45 Gray Reload

K190999 Class II Traditional
Decision Date
2019-07-12
Sponsor / Applicant
Intuitive Surgical, Inc.

Technical Specification

510(k) Submission ID K190999
Product Code NAY
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2019-07-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SureForm 45 Curved Tip, SureForm 45 Gray Reload received FDA 510(k) clearance under submission number K190999, 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 2019-07-12.

Classification & Regulation

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