meddevicedb.com FDA Device Reference

COOL LINE CATHETER KIT, MODELS CL-2085B, CL-2295A; ICY CATHETER KIT, MODEL IC-3585A; FORTIUS CATHETER KIT, MOD. FR-5093B

K051912 Class II Traditional
Decision Date
2005-10-11
Sponsor / Applicant
Alsius Corp.

Technical Specification

510(k) Submission ID K051912
Product Code NCX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5900
Decision Date 2005-10-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COOL LINE CATHETER KIT, MODELS CL-2085B, CL-2295A; ICY CATHETER KIT, MODEL IC-3585A; FORTIUS CATHETER KIT, MOD. FR-5093B received FDA 510(k) clearance under submission number K051912, sponsored by Alsius Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2005-10-11.

Classification & Regulation

This clearance is catalogued under FDA product code NCX and 21 CFR 870.5900, within the Cardiovascular review panel as a Class II device.