meddevicedb.com FDA Device Reference

Citrasate Liquid Acid Concentrate, NaturaLyte Liquid Acid Concentrate

K212620 Class II Traditional
Decision Date
2022-05-12
Sponsor / Applicant
Fresenius Medical Care Renal Therapies Group, LLC

Technical Specification

510(k) Submission ID K212620
Product Code KPO
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 2022-05-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Citrasate Liquid Acid Concentrate, NaturaLyte Liquid Acid Concentrate received FDA 510(k) clearance under submission number K212620, sponsored by Fresenius Medical Care Renal 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 2022-05-12.

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.