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DIALYSATE CONCENTRATE FOR HEMODIALYSIS-LIQUID/POWD

K843963 Class II Traditional
Decision Date
1985-01-07
Sponsor / Applicant
Renal Systems, Inc.

Technical Specification

510(k) Submission ID K843963
Product Code FKQ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1985-01-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIALYSATE CONCENTRATE FOR HEMODIALYSIS-LIQUID/POWD received FDA 510(k) clearance under submission number K843963, sponsored by Renal Systems, Inc.. 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 1985-01-07.

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.