Class Class II
NIDO Baby Magnetic Resonance Imaging System (K242573)
Description
NIDO Baby Magnetic Resonance Imaging System by Jiangsu Lici Medical Device Co., Ltd., an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242573
Clearance Date2024-12-23
Clearance TypeTraditional
Product CodeLNH
Regulation Number892.1000
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242573
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. NIDO Baby Magnetic Resonance Imaging System (K242573) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K192002 | Lucy Point-of-Care Magnetic Resonance Imaging Device | Hyperfine Research, Inc. | 2020 |
| K170978 | Embrace Neonatal MRI System | Aspect Imaging, Ltd. | 2017 |
Trace the full predicate network for K242573
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.