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FDA 510(k)

NIDO Baby Magnetic Resonance Imaging System

K-Number: K242573 · 2024-12-23

ApplicantJiangsu Lici Medical Device Co., Ltd.
Decision Date2024-12-23
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

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. It is manufactured by Jiangsu Lici Medical Device Co., Ltd.. The 510(k) number is K242573.

When was NIDO Baby Magnetic Resonance Imaging System approved by the FDA?

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

What company makes NIDO Baby Magnetic Resonance Imaging System?

NIDO Baby Magnetic Resonance Imaging System is manufactured by Jiangsu Lici Medical Device Co., Ltd..

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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Related PubMed Literature

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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