meddevicedb.com FDA Device Reference

URESIL IRRIGATION CATHETER

K863564 Class II Traditional
Decision Date
1986-10-10
Sponsor / Applicant
Uresil Corp.

Technical Specification

510(k) Submission ID K863564
Product Code DQY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 1986-10-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

URESIL IRRIGATION CATHETER received FDA 510(k) clearance under submission number K863564, sponsored by Uresil 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 1986-10-10.

Classification & Regulation

This clearance is catalogued under FDA product code DQY and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.