meddevicedb.com FDA Device Reference

ICE Aspiration System

K234073 Class II Traditional
Decision Date
2024-04-19
Sponsor / Applicant
Expanse Medical, Inc.

Technical Specification

510(k) Submission ID K234073
Product Code QEW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5150
Decision Date 2024-04-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ICE Aspiration System received FDA 510(k) clearance under submission number K234073, sponsored by Expanse Medical, 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 2024-04-19.

Classification & Regulation

This clearance is catalogued under FDA product code QEW and 21 CFR 870.5150, within the Cardiovascular review panel as a Class II device.