ClearanceBrief
510(k) K091534 ยท HQF Laser, Ophthalmic

LIGHTLAS MODEL 532

ApplicantLightmed Corp., Taipei, TW
DecisionSubstantially Equivalent, Sep 18, 2009
ReceivedMay 26, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K091534

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.