meddevicedb.com FDA Device Reference

IC-Flow™ Imaging System 2.0

K243645 Class II Traditional
Decision Date
2025-09-22
Sponsor / Applicant
Diagnostic Green GmbH

Technical Specification

510(k) Submission ID K243645
Product Code IZI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1600
Decision Date 2025-09-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IC-Flow™ Imaging System 2.0 received FDA 510(k) clearance under submission number K243645, sponsored by Diagnostic Green GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2025-09-22.

Classification & Regulation

This clearance is catalogued under FDA product code IZI and 21 CFR 892.1600, within the Radiology review panel as a Class II device.