meddevicedb.com FDA Device Reference

FLOWRUNNER Aspiration System

K254208 Class II Special
Decision Date
2026-03-20
Sponsor / Applicant
Expanse Medical, Inc.

Technical Specification

510(k) Submission ID K254208
Product Code QEZ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5150
Decision Date 2026-03-20
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLOWRUNNER Aspiration System received FDA 510(k) clearance under submission number K254208, sponsored by Expanse Medical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2026-03-20.

Classification & Regulation

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