K240314
- 510(k) number
- K240314
- Device name
- MULA (K2-A1)
- Applicant
- Guangzhou Ciellulu Photoelectric Technology Co., Ltd. CN
- Product code
- ONF — Powered Light Based Non-Laser Surgical Instrument Wi
- Decision date
- 2024-08-21
- Date received
- 2024-02-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K240314.pdf
Official FDA record: K240314
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.