Class Class II
AeviceMD (K243603)
Description
AeviceMD by Aevice Health Pte. , Ltd., an FDA 510(k) cleared cardiovascular device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK243603
Clearance Date2025-05-05
Clearance TypeTraditional
Product CodeDSH
Regulation Number870.2800
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K243603
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. AeviceMD (K243603) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K223382 | AeviceMD | Aevice Health Pte. , Ltd. | 2023 |
| K200776 | Eko CORE | Eko Devices, Inc. | 2020 |
Trace the full predicate network for K243603
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.