ClearanceBrief
510(k) K090633 ยท OOE Ophthalmic Femtosecond Laser

LENSAR LASER SYSTEM

ApplicantLensar, Inc., Winter Park FL, US
DecisionSubstantially Equivalent, May 13, 2010
ReceivedMar 9, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090633

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.