Class Class II
Fetal EchoScan (v1.1) (K251071)
Description
Fetal EchoScan (v1.1) by Brightheart, an FDA 510(k) cleared radiology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK251071
Clearance Date2025-05-02
Clearance TypeSpecial
Product CodePOK
Regulation Number892.2060
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K251071
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. Fetal EchoScan (v1.1) (K251071) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K242342 | Fetal EchoScan | Brightheart | 2024 |
Trace the full predicate network for K251071
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.