FDA 510(k)

NIDO Baby Magnetic Resonance Imaging System

Número K: K242573 · 2024-12-23

RequerenteJiangsu Lici Medical Device Co., Ltd.

Data da decisão2024-12-23

Código do produtoLNH

Comité consultivoRA

DecisãoSubstantially Equivalent

Resumo do 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.

Perguntas frequentes

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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