Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MULA (K2-A1)

K-Number: K240314 · 2024-08-21

ApplicantGuangzhou Ciellulu Photoelectric Technology Co., Ltd.
Decision Date2024-08-21
Product CodeONF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MULA (K2-A1) is a medical device manufactured by Guangzhou Ciellulu Photoelectric Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-08-21 under approval number K240314. The device is classified under product code ONF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULA (K2-A1)?

MULA (K2-A1) is a medical device that received FDA 510(k) clearance on 2024-08-21. It is manufactured by Guangzhou Ciellulu Photoelectric Technology Co., Ltd.. The 510(k) number is K240314.

When was MULA (K2-A1) approved by the FDA?

MULA (K2-A1) received FDA 510(k) clearance on 2024-08-21, under approval number K240314.

What company makes MULA (K2-A1)?

MULA (K2-A1) is manufactured by Guangzhou Ciellulu Photoelectric Technology Co., Ltd..

What is the FDA product code for MULA (K2-A1)?

The FDA product code for MULA (K2-A1) is ONF.

Related Devices (Code: ONF)

K161565DUOStetic Medical Aesthetics Development (Shenzhen) Co. ,Ltd K161286IPL Therapy MachineBeijing Adss Development Co., Ltd. K160195Forma System, Forma Light SystemFormatk Systems , Ltd. K153717Venus Versa SystemVenus Concept , Ltd. K152790Venus Versa SystemVenus Concept , Ltd. K181868SHINY RPL SystemIds, Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑