meddevicedb.com FDA Device Reference

Magnifico Open (100009900)

K251901 Class II Traditional
Decision Date
2026-03-05
Sponsor / Applicant
Esaote, S.p.A.

Technical Specification

510(k) Submission ID K251901
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2026-03-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Magnifico Open (100009900) received FDA 510(k) clearance under submission number K251901, sponsored by Esaote, S.p.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2026-03-05.

Classification & Regulation

This clearance is catalogued under FDA product code LNH and 21 CFR 892.1000, within the Radiology review panel as a Class II device.