meddevicedb.com FDA Device Reference

Embrace Neonatal MRI System

K254277 Class II Traditional
Decision Date
2026-03-13
Sponsor / Applicant
Aspect Imaging, Ltd.

Technical Specification

510(k) Submission ID K254277
Product Code LNH
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1000
Decision Date 2026-03-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Embrace Neonatal MRI System received FDA 510(k) clearance under submission number K254277, sponsored by Aspect Imaging, 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 2026-03-13.

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.