S90 Exp Series Digital Color Doppler Ultrasound System (K222596)
Description
S90 Exp Series Digital Color Doppler Ultrasound System by Sonoscape Medical Corp., an FDA 510(k) cleared radiology device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K222596
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. S90 Exp Series Digital Color Doppler Ultrasound System (K222596) cites 3 predicate devices and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K210053 | LVivo Software Application | Dia Imaging Analysis, Ltd. | 2021 |
| K201059 | S60 Elite Series/S70 Series Digital Color Doppler Ultrasoun... | Sonoscape Medical Corp. | 2020 |
| K171000 | P60 Series Digital Color Doppler Ultrasound System | Sonoscape Medical Corp. | 2017 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K241949 | Digital Color Doppler Ultrasound System (P60 Series) | Sonoscape Medical Corp. | 2025 |
Trace the full predicate network for K222596
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.