ClearanceBrief
510(k) K123831 ยท OKS Lacrimal Stents And Intubation Sets

OPHTACATH KIT

ApplicantFrance Chirurgae Instrumentation, Cincinnati OH, US
DecisionSubstantially Equivalent, Jul 29, 2013
ReceivedDec 12, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123831

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.