Class Class II
MI View&GO (K242300)
Description
MI View&GO by Siemens Medical Solutions USA, Inc., an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242300
Clearance Date2024-08-30
Clearance TypeSpecial
Product CodeQIH
Regulation Number892.2050
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242300
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. MI View&GO (K242300) cites 2 predicate devices and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K222172 | MI View&GO | Siemens Medical Solutions USA, Inc. | 2022 |
| K201202 | MI View&GO | Siemens Medical Solutions USA, Inc. | 2020 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K251561 | Biograph Trinion | Siemens Medical Solutions USA, Inc. | 2025 |
Trace the full predicate network for K242300
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.