Class Class II
RHYTHMIA HDx™ Mapping System (K241227)
Description
RHYTHMIA HDx™ Mapping System by Boston Scientific Corporation, an FDA 510(k) cleared cardiovascular device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK241227
Clearance Date2024-08-29
Clearance TypeTraditional
Product CodeDQK
Regulation Number870.1425
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K241227
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. RHYTHMIA HDx™ Mapping System (K241227) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K192438 | Rhythmia HDxTM Mapping System | Boston Scientific Corporation | 2019 |
| K162793 | RHYTHMIA HDx Mapping System | Boston Scientific Corporation | 2017 |
Trace the full predicate network for K241227
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.