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HEMODIALYSIS BLOOD CIRCUIT

K790591 Class II Traditional
Decision Date
1979-05-02
Sponsor / Applicant
Travenol Laboratories, S.A.

Technical Specification

510(k) Submission ID K790591
Product Code KOC
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1979-05-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEMODIALYSIS BLOOD CIRCUIT received FDA 510(k) clearance under submission number K790591, 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 1979-05-02.

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.