Class Class II
Revian Lyte (10011) (K242441)
Description
Revian Lyte (10011) by Revian, Inc., an FDA 510(k) cleared physical medicine device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242441
Clearance Date2024-09-13
Clearance TypeSpecial
Product CodeOAP
Regulation Number890.5500
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242441
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. Revian Lyte (10011) (K242441) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K190467 | iHelmet Hair Growth System | Slinph Technologies Co., Ltd. | 2019 |
| K173729 | REVIAN RED | Photonmd, Inc. | 2018 |
Trace the full predicate network for K242441
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.