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EXTRACORPOREAL BLOOD CIRCUIT

K982340 Class II Traditional
Decision Date
1999-04-30
Sponsor / Applicant
Haidylena Medical Egypt

Technical Specification

510(k) Submission ID K982340
Product Code FJK
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1999-04-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXTRACORPOREAL BLOOD CIRCUIT received FDA 510(k) clearance under submission number K982340, sponsored by Haidylena Medical Egypt. 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 1999-04-30.

Classification & Regulation

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