meddevicedb.com FDA Device Reference

MEDIVATORS™ ADVANTAGE NXT™ Automated Endoscope Reprocessor

K261791 Class II Traditional
Decision Date
2026-10-02
Sponsor / Applicant
Steris

Technical Specification

510(k) Submission ID K261791
Product Code FEB
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2026-10-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDIVATORS™ ADVANTAGE NXT™ Automated Endoscope Reprocessor received FDA 510(k) clearance under submission number K261791, sponsored by Steris. 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 2026-10-02.

Classification & Regulation

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