ClearanceBrief
510(k) K013646 ยท HQD Lens, Contact (Other Material) - Daily

ROSE K POST GRAFT LENS

ApplicantRose K International , Ltd., Hamilton, NZ
DecisionSubstantially Equivalent, May 30, 2002
ReceivedNov 5, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K013646

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.