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Scope-Assist Flushing Sink

K162120 Class II Traditional
Decision Date
2017-04-28
Sponsor / Applicant
Custom Ultrasonics, Inc.

Technical Specification

510(k) Submission ID K162120
Product Code FEB
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2017-04-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Scope-Assist Flushing Sink received FDA 510(k) clearance under submission number K162120, sponsored by Custom Ultrasonics, 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 2017-04-28.

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.