Class Class II
MEDIYAG (K231948)
Description
MEDIYAG by Medicreations, LLC, an FDA 510(k) cleared general, plastic surgery device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK231948
Clearance Date2024-10-09
Clearance TypeSpecial
Product CodeGEX
Regulation Number878.4810
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K231948
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. MEDIYAG (K231948) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K193477 | Nd: YAG Laser Therapy Systems | Beijing Kes Biology Technology Co.,... | 2020 |
| K161926 | ND YAG Q-switch Laser Therapy Machine | Beijing Adss Development Co., Ltd. | 2017 |
Trace the full predicate network for K231948
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.