meddevicedb.com FDA Device Reference

FLOWRUNNER Aspiration System

K251488 Class II Special
Decision Date
2025-07-14
Sponsor / Applicant
Expanse Medical, Inc.

Technical Specification

510(k) Submission ID K251488
Product Code QEZ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5150
Decision Date 2025-07-14
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 K251488, 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 2025-07-14.

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.