meddevicedb.com FDA Device Reference

POWER-TRIALYSIS TRIPLE LUMEN ACUTE DIALYSIS CATHETER

K083675 Class II Traditional
Decision Date
2009-03-19
Sponsor / Applicant
C.R. Bard, Inc.

Technical Specification

510(k) Submission ID K083675
Product Code NIE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5540
Decision Date 2009-03-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWER-TRIALYSIS TRIPLE LUMEN ACUTE DIALYSIS CATHETER received FDA 510(k) clearance under submission number K083675, sponsored by C.R. Bard, Inc.. 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 2009-03-19.

Classification & Regulation

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