meddevicedb.com FDA Device Reference

Senhance Surgical System

K223095 Class II Traditional
Decision Date
2023-03-16
Sponsor / Applicant
Asensus Surgical, Inc.

Technical Specification

510(k) Submission ID K223095
Product Code NAY
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2023-03-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Senhance Surgical System received FDA 510(k) clearance under submission number K223095, sponsored by Asensus 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 2023-03-16.

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.