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HEMODIALYSIS CONCENTRATES & RELATED PRODUCTS

K870979 Class II Traditional
Decision Date
1987-06-03
Sponsor / Applicant
Inventory Supply Corp.

Technical Specification

510(k) Submission ID K870979
Product Code KPO
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1987-06-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMODIALYSIS CONCENTRATES & RELATED PRODUCTS received FDA 510(k) clearance under submission number K870979, sponsored by Inventory Supply 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 1987-06-03.

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.