K233018
- 510(k) number
- K233018
- Device name
- PICOSECOND Nd:YAG Laser System
- Applicant
- Ids, Ltd. KR
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2023-12-21
- Date received
- 2023-09-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K233018.pdf
Official FDA record: K233018
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.