FDA 510(k)

NIDO Baby Magnetic Resonance Imaging System

N.º K: K242573 · 2024-12-23

SolicitanteJiangsu Lici Medical Device Co., Ltd.

Fecha de decisión2024-12-23

Código de productoLNH

Comité asesorRA

DecisiónSubstantially Equivalent

Resumen del dispositivo

NIDO Baby Magnetic Resonance Imaging System is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Lici Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2024-12-23 under 510(k) number K242573. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Preguntas frecuentes

What is the NIDO Baby Magnetic Resonance Imaging System?

NIDO Baby Magnetic Resonance Imaging System is a medical device that received FDA 510(k) clearance on 2024-12-23. The listed applicant is Jiangsu Lici Medical Device Co., Ltd.. The 510(k) number is K242573.

When did NIDO Baby Magnetic Resonance Imaging System receive FDA 510(k) clearance?

NIDO Baby Magnetic Resonance Imaging System received FDA 510(k) clearance on 2024-12-23, under 510(k) number K242573.

Who is the listed applicant for NIDO Baby Magnetic Resonance Imaging System?

The FDA 510(k) record lists Jiangsu Lici Medical Device Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NIDO Baby Magnetic Resonance Imaging System?

The FDA product code for NIDO Baby Magnetic Resonance Imaging System is LNH.

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Fuente oficial

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