Class Class II
EchoSolv AS (K241245)
Description
EchoSolv AS by Echo IQ, Ltd., an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK241245
Clearance Date2024-10-04
Clearance TypeTraditional
Product CodePOK
Regulation Number892.2060
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241245
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. EchoSolv AS (K241245) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K201555 | EchoGo Pro | Ultromics, Ltd. | 2020 |
Trace the full predicate network for K241245
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.