ClearanceBrief
510(k) K230350 ยท HQF Laser, Ophthalmic

VISULAS yag

ApplicantCarl Zeiss Meditec, Inc., Dublin CA, US
DecisionSubstantially Equivalent, Sep 22, 2023
ReceivedFeb 9, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230350

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.