K260895
- 510(k) number
- K260895
- Device name
- Ulike Clear Zero (YC10 BU)
- Applicant
- Guangxi Ulike Medical Technology Co., Ltd. CN
- Product code
- NFO — Stimulator, Transcutaneous Electrical, Aesthetic Pur
- Decision date
- 2026-05-28
- Date received
- 2026-03-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
510(k) Summary (official FDA PDF): K260895.pdf
Official FDA record: K260895
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.