meddevicedb.com FDA Device Reference

Velacur One (LI-1100)

K251728 Class II Special
Decision Date
2025-06-26
Sponsor / Applicant
Sonic Incytes Medical Corp

Technical Specification

510(k) Submission ID K251728
Product Code IYO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1560
Decision Date 2025-06-26
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Velacur One (LI-1100) received FDA 510(k) clearance under submission number K251728, sponsored by Sonic Incytes Medical Corp. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2025-06-26.

Classification & Regulation

This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.