meddevicedb.com FDA Device Reference

HEMODIALYSIS CONCENTRATES

K883068 Class II Traditional
Decision Date
1988-12-22
Sponsor / Applicant
Dove Medical Supplies

Technical Specification

510(k) Submission ID K883068
Product Code KPO
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1988-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMODIALYSIS CONCENTRATES received FDA 510(k) clearance under submission number K883068, sponsored by Dove Medical Supplies. 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 1988-12-22.

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.