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INFUSION CATHETER EXTENSION SET

K023224 Class II Special
Decision Date
2002-10-25
Sponsor / Applicant
Chf Solutions, Inc.

Technical Specification

510(k) Submission ID K023224
Product Code KDI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5860
Decision Date 2002-10-25
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INFUSION CATHETER EXTENSION SET received FDA 510(k) clearance under submission number K023224, sponsored by Chf Solutions, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2002-10-25.

Classification & Regulation

This clearance is catalogued under FDA product code KDI and 21 CFR 876.5860, within the Gastroenterology, Urology review panel as a Class II device.