510(k) K251507

Device
INTEGRE LIO
Applicant
Quantel Medical
510(k) number
K251507
Product code
HQF
Decision
Substantially Equivalent (SESE)
Decision date
2026-02-06
Date received
2025-05-16
Regulation
886.4390
Classification name
Laser, Ophthalmic
Medical specialty
Ophthalmic
Review panel
Ophthalmic
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Bruno Pages
Address
1 Rue Du Bois Joli Cs40015 Cournon D'Auvergne-Cedex FR 63808 63808

FDA Registration Numbers

Source Documents

510(k) summary PDF

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