meddevicedb.com FDA Device Reference

1688 4K Camera System with Advanced Imaging Modality; 1788 4K Camera System with Advanced Imaging Modality

K260185 Class II Special
Decision Date
2026-02-18
Sponsor / Applicant
Stryker Endoscopy

Technical Specification

510(k) Submission ID K260185
Product Code GCJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2026-02-18
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

1688 4K Camera System with Advanced Imaging Modality; 1788 4K Camera System with Advanced Imaging Modality received FDA 510(k) clearance under submission number K260185, sponsored by Stryker Endoscopy. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2026-02-18.

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.