meddevicedb.com FDA Device Reference

Magnifico Open (100009900); Magnifico MSK ( 100009910)

K241133 Class II Special
Decision Date
2024-06-26
Sponsor / Applicant
Esaote, S.p.A.

Technical Specification

510(k) Submission ID K241133
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2024-06-26
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Magnifico Open (100009900); Magnifico MSK ( 100009910) received FDA 510(k) clearance under submission number K241133, sponsored by Esaote, S.p.A.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2024-06-26.

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.