meddevicedb.com FDA Device Reference

Foresight Intracardiac Echocardiography (ICE) System

K151126 Class II Traditional
Decision Date
2015-12-18
Sponsor / Applicant
Colibri Technologies, Inc.

Technical Specification

510(k) Submission ID K151126
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 2015-12-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Foresight Intracardiac Echocardiography (ICE) System received FDA 510(k) clearance under submission number K151126, sponsored by Colibri Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2015-12-18.

Classification & Regulation

This clearance is catalogued under FDA product code DQO and 21 CFR 870.1200, within the Cardiovascular review panel as a Class II device.