Class Class II
DCM (PW-DCM) (K243513)
Description
DCM (PW-DCM) by Pneumowave, Ltd., an FDA 510(k) cleared neurology device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK243513
Clearance Date2025-04-16
Clearance TypeTraditional
Product CodeLEL
Regulation Number882.5050
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K243513
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. DCM (PW-DCM) (K243513) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K231532 | ActiGraph LEAP activity monitor (ActiGraph LEAP) | Actigraph, LLC | 2023 |
| K132764 | MOTION WATCH AND PRO-DIARY | Camntech, Ltd. | 2014 |
Trace the full predicate network for K243513
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.