Class Class II
WHILL Model R (K242760)
Description
WHILL Model R by Whill, Inc., an FDA 510(k) cleared physical medicine device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242760
Clearance Date2025-01-06
Clearance TypeTraditional
Product CodeINI
Regulation Number890.3800
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242760
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. WHILL Model R (K242760) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K222495 | Mobility Scooter, Model: W3331F | Zhejiang Innuovo Rehabilitation Dev... | 2022 |
| K221438 | WHILL Model F | Whill, Inc. | 2022 |
Trace the full predicate network for K242760
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.