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AUTOMATIC PERITONEAL DIALYSIS CYCLER SET (5C4437)

K873984 Class II Traditional
Decision Date
1987-10-20
Sponsor / Applicant
Travenol Laboratories, S.A.

Technical Specification

510(k) Submission ID K873984
Product Code KDJ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5630
Decision Date 1987-10-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUTOMATIC PERITONEAL DIALYSIS CYCLER SET (5C4437) received FDA 510(k) clearance under submission number K873984, 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 1987-10-20.

Classification & Regulation

This clearance is catalogued under FDA product code KDJ and 21 CFR 876.5630, within the Gastroenterology, Urology review panel as a Class II device.