meddevicedb.com FDA Device Reference

HEMODIALYSIS CONCENTRATE FORMULATIONS/ADDITIVES

K860297 Class II Traditional
Decision Date
1986-03-04
Sponsor / Applicant
Renal Hygienics

Technical Specification

510(k) Submission ID K860297
Product Code FKQ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1986-03-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMODIALYSIS CONCENTRATE FORMULATIONS/ADDITIVES received FDA 510(k) clearance under submission number K860297, sponsored by Renal Hygienics. 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 1986-03-04.

Classification & Regulation

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