FDA 510(k)

Ascent3T Neonatal Magnetic Resonance Imaging System

Número K: K253499 · 2026-01-26

Data da decisão2026-01-26

Código do produtoLNH

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do dispositivo

Ascent3T Neonatal Magnetic Resonance Imaging System is the device name listed in this FDA 510(k) record. The listed applicant is Eyas Medical Imaging, Inc.. It received FDA 510(k) clearance on 2026-01-26 under 510(k) number K253499. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Perguntas frequentes

What is the Ascent3T Neonatal Magnetic Resonance Imaging System?

Ascent3T Neonatal Magnetic Resonance Imaging System is a medical device that received FDA 510(k) clearance on 2026-01-26. The listed applicant is Eyas Medical Imaging, Inc.. The 510(k) number is K253499.

When did Ascent3T Neonatal Magnetic Resonance Imaging System receive FDA 510(k) clearance?

Ascent3T Neonatal Magnetic Resonance Imaging System received FDA 510(k) clearance on 2026-01-26, under 510(k) number K253499.

Who is the listed applicant for Ascent3T Neonatal Magnetic Resonance Imaging System?

The FDA 510(k) record lists Eyas Medical Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ascent3T Neonatal Magnetic Resonance Imaging System?

The FDA product code for Ascent3T Neonatal Magnetic Resonance Imaging System is LNH.

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