meddevicedb.com FDA Device Reference

Handheld Ultrasound Scanner

K261288 Class II Traditional
Decision Date
2026-07-30
Sponsor / Applicant
IMGFAX CO., LTD.

Technical Specification

510(k) Submission ID K261288
Product Code IYN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1550
Decision Date 2026-07-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Handheld Ultrasound Scanner received FDA 510(k) clearance under submission number K261288, sponsored by IMGFAX CO., LTD.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2026-07-30.

Classification & Regulation

This clearance is catalogued under FDA product code IYN and 21 CFR 892.1550, within the Radiology review panel as a Class II device.