K233224
- 510(k) number
- K233224
- Device name
- Epilaser Pro
- Applicant
- Epilady 2000, LLC IL
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2024-01-27
- Date received
- 2023-09-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K233224.pdf
Official FDA record: K233224
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.