meddevicedb.com FDA Device Reference

Citric Complete Liquid Citric Acid Concentrate

K223431 Class II Traditional
Decision Date
2023-08-04
Sponsor / Applicant
Nipro Renal Solutions USA, Corp.

Technical Specification

510(k) Submission ID K223431
Product Code KPO
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 2023-08-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Citric Complete Liquid Citric Acid Concentrate received FDA 510(k) clearance under submission number K223431, sponsored by Nipro Renal Solutions USA, Corp.. 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 2023-08-04.

Classification & Regulation

This clearance is catalogued under FDA product code KPO and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.