meddevicedb.com FDA Device Reference

Diversatek Healthcare PureFlo Irrigation System / Water Bottle Tubing

K222734 Class II Traditional
Decision Date
2022-11-08
Sponsor / Applicant
Diversatek Healthcare

Technical Specification

510(k) Submission ID K222734
Product Code OCX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 2022-11-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Diversatek Healthcare PureFlo Irrigation System / Water Bottle Tubing received FDA 510(k) clearance under submission number K222734, sponsored by Diversatek Healthcare. 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 2022-11-08.

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.