meddevicedb.com FDA Device Reference

CASCADE HEMODIALYSIS/APHERESIS CATHETER

K130851 Class II Traditional
Decision Date
2014-01-09
Sponsor / Applicant
Health Line International Corporation

Technical Specification

510(k) Submission ID K130851
Product Code MSD
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5540
Decision Date 2014-01-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CASCADE HEMODIALYSIS/APHERESIS CATHETER received FDA 510(k) clearance under submission number K130851, sponsored by Health Line International Corporation. 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 2014-01-09.

Classification & Regulation

This clearance is catalogued under FDA product code MSD and 21 CFR 876.5540, within the Gastroenterology, Urology review panel as a Class II device.