Class Class II
Apollo TMS Therapy System (K243539)
Description
Apollo TMS Therapy System by Mag & More GmbH, an FDA 510(k) cleared neurology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK243539
Clearance Date2025-08-18
Clearance TypeTraditional
Product CodeOBP
Regulation Number882.5805
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K243539
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. Apollo TMS Therapy System (K243539) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K232639 | Apollo TMS Therapy System | Mag & More GmbH | 2024 |
| K222171 | Magstim Horizon 3.0 TMS Therapy System, Horizon 3.0 System,... | Magstim Company, Ltd. | 2023 |
Trace the full predicate network for K243539
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.