Class Class II
RFMagik Lite (K242469)
Description
RFMagik Lite by Agnes Medical Co., Ltd., an FDA 510(k) cleared general, plastic surgery device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242469
Clearance Date2025-04-25
Clearance TypeTraditional
Product CodeGEI
Regulation Number878.4400
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242469
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. RFMagik Lite (K242469) cites 2 predicate devices and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K231216 | POTENZA | Jeisys Medical, Inc. | 2024 |
| K223805 | Agnes | Agnes Medical Co., Ltd. | 2023 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K243713 | Single Use RF Surgical Electrode (Needle Type) (AN-B, AN-C,... | Agnes Medical Co., Ltd. | 2025 |
Trace the full predicate network for K242469
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.