meddevicedb.com FDA Device Reference

System 83 Plus Washer/Disinfector

K173590 Class II Traditional
Decision Date
2020-03-30
Sponsor / Applicant
Custom Ultrasonics, Inc.

Technical Specification

510(k) Submission ID K173590
Product Code FEB
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2020-03-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

System 83 Plus Washer/Disinfector received FDA 510(k) clearance under submission number K173590, 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 2020-03-30.

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.