Class Class II
Volta AF-Xplorer (K243812)
Description
Volta AF-Xplorer by Volta Medical, an FDA 510(k) cleared cardiovascular device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK243812
Clearance Date2025-05-09
Clearance TypeTraditional
Product CodeDQK
Regulation Number870.1425
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K243812
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. Volta AF-Xplorer (K243812) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K232616 | Volta AF-Xplorer | Volta Medical | 2023 |
| K201298 | VX1 | Volta Medical | 2020 |
Trace the full predicate network for K243812
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.