ClearanceBrief
510(k) K181430 ยท OOE Ophthalmic Femtosecond Laser

LENSAR Laser System - fs 3D (LLS-fs 3D)

ApplicantLensar, Inc., Orlando FL, US
DecisionSubstantially Equivalent, Aug 9, 2018
ReceivedJun 1, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K181430

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.