meddevicedb.com FDA Device Reference

POWERPICC CATHETERS, MODELS 3175155, 3175135

K033389 Class II Traditional
Decision Date
2004-03-19
Sponsor / Applicant
C.R. Bard, Inc.

Technical Specification

510(k) Submission ID K033389
Product Code LJS
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5970
Decision Date 2004-03-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

POWERPICC CATHETERS, MODELS 3175155, 3175135 received FDA 510(k) clearance under submission number K033389, sponsored by C.R. Bard, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2004-03-19.

Classification & Regulation

This clearance is catalogued under FDA product code LJS and 21 CFR 880.5970, within the General Hospital review panel as a Class II device.