510(k) K123859 · OOE Ophthalmic Femtosecond Laser

TBD

Applicant	Lensar, Inc., Orlando FL, US
Decision	Substantially Equivalent, Mar 27, 2013
Received	Dec 14, 2012
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K123859

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.