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LOW-ACETATE HEMODIALYSIS BATH CONCENTR.

K800624 Class II Traditional
Decision Date
1980-07-14
Sponsor / Applicant
Travenol Laboratories, S.A.

Technical Specification

510(k) Submission ID K800624
Product Code KPO
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1980-07-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LOW-ACETATE HEMODIALYSIS BATH CONCENTR. received FDA 510(k) clearance under submission number K800624, sponsored by Travenol Laboratories, S.A.. 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 1980-07-14.

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.