ClearanceBrief
510(k) K023045 ยท LXS Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla

MICRORUPTER V

ApplicantMeridian AG, Thun, Bern, CH
DecisionSubstantially Equivalent, Sep 26, 2002
ReceivedSep 12, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K023045

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.