K243014
- 510(k) number
- K243014
- Device name
- EyeQ nanoECP
- Applicant
- Eyeq, Inc. NV · US
- Product code
- HQF — Laser, Ophthalmic
- Decision date
- 2025-06-18
- Date received
- 2024-09-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ophthalmic
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K243014
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.