K251507
- 510(k) number
- K251507
- Device name
- INTEGRE LIO
- Applicant
- Quantel Medical FR
- Product code
- HQF — Laser, Ophthalmic
- Decision date
- 2026-02-06
- Date received
- 2025-05-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Ophthalmic
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K251507.pdf
Official FDA record: K251507
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.