meddevicedb.com FDA Device Reference

Y-CLICK CONNECTOR

K060759 Class II Traditional
Decision Date
2006-06-29
Sponsor / Applicant
Elcam Medical Acal

Technical Specification

510(k) Submission ID K060759
Product Code DTL
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4290
Decision Date 2006-06-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Y-CLICK CONNECTOR received FDA 510(k) clearance under submission number K060759, sponsored by Elcam Medical Acal. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2006-06-29.

Classification & Regulation

This clearance is catalogued under FDA product code DTL and 21 CFR 870.4290, within the Cardiovascular review panel as a Class II device.