ClearanceBrief
510(k) K030353 ยท OKS Lacrimal Stents And Intubation Sets

MONOCANALICULAR STENTS, LACRIMAL INTUBATION SETS

ApplicantEagle Vision, Inc., Memphis TN, US
DecisionSubstantially Equivalent, Apr 25, 2003
ReceivedFeb 3, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030353

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.