meddevicedb.com FDA Device Reference

AquaA

K213507 Class II Traditional
Decision Date
2022-07-27
Sponsor / Applicant
Fresenius Medical Care Rental Therapies Group, LLC

Technical Specification

510(k) Submission ID K213507
Product Code FIP
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5665
Decision Date 2022-07-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AquaA received FDA 510(k) clearance under submission number K213507, sponsored by Fresenius Medical Care Rental Therapies Group, LLC. 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 2022-07-27.

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.