meddevicedb.com FDA Device Reference

troCarWash™ System

K233442 Class II Traditional
Decision Date
2024-05-21
Sponsor / Applicant
Biotex, Inc.

Technical Specification

510(k) Submission ID K233442
Product Code OCX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2024-05-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

troCarWash™ System received FDA 510(k) clearance under submission number K233442, sponsored by Biotex, 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 2024-05-21.

Classification & Regulation

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