meddevicedb.com FDA Device Reference

AquaC UNO H

K143617 Class II Traditional
Decision Date
2015-10-19
Sponsor / Applicant
Vivonic GmbH

Technical Specification

510(k) Submission ID K143617
Product Code FIP
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5665
Decision Date 2015-10-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AquaC UNO H received FDA 510(k) clearance under submission number K143617, sponsored by Vivonic GmbH. 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 2015-10-19.

Classification & Regulation

This clearance is catalogued under FDA product code FIP and 21 CFR 876.5665, within the Gastroenterology, Urology review panel as a Class II device.