Class Class II
DEEPECHO (K242594)
Description
DEEPECHO by Deepecho, an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242594
Clearance Date2025-05-23
Clearance TypeTraditional
Product CodeIYN
Regulation Number892.1550
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242594
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. DEEPECHO (K242594) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K230365 | Sonio Detect | Sonio | 2023 |
| K223387 | V8 Diagnostic Ultrasound System, V7 Diagnostic Ultrasound S... | Samsung Medison Co., Ltd. | 2023 |
Trace the full predicate network for K242594
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.