Class Class II
MULA (K2-A1) (K240314)
Description
MULA (K2-A1) by Guangzhou Ciellulu Photoelectric Technology Co., Ltd., an FDA 510(k) cleared general, plastic surgery device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK240314
Clearance Date2024-08-21
Clearance TypeTraditional
Product CodeONF
Regulation Number878.4810
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K240314
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. MULA (K2-A1) (K240314) cites 2 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K193072 | Lucent : IPL | Luvo Medical Technologies, Inc. | 2020 |
| K193500 | Stellar M22 for Intense Pulsed Light (IPL) and Laser System | Lumenis, Ltd. | 2020 |
Trace the full predicate network for K240314
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.