meddevicedb.com FDA Device Reference

HEMODIALYSATE SOLUTIONS

K843866 Class II Traditional
Decision Date
1985-01-09
Sponsor / Applicant
Bicarbolyte Corp.

Technical Specification

510(k) Submission ID K843866
Product Code KPO
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1985-01-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMODIALYSATE SOLUTIONS received FDA 510(k) clearance under submission number K843866, sponsored by Bicarbolyte 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 1985-01-09.

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.