meddevicedb.com FDA Device Reference

DIALYSIS PRIMING SETS CODES 5C4094 AND 5C4095

K896006 Class II Traditional
Decision Date
1989-12-27
Sponsor / Applicant
Baxter Healthcare Corp

Technical Specification

510(k) Submission ID K896006
Product Code KOC
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1989-12-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIALYSIS PRIMING SETS CODES 5C4094 AND 5C4095 received FDA 510(k) clearance under submission number K896006, sponsored by Baxter Healthcare 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 1989-12-27.

Classification & Regulation

This clearance is catalogued under FDA product code KOC and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.