ClearanceBrief
510(k) K121142 ยท OKS Lacrimal Stents And Intubation Sets

CRAWFORD BIOCANALICULUS INTUBATION

ApplicantFci Sas (France Chirurgie Instrumentation), Cincinnati OH, US
DecisionSubstantially Equivalent, Aug 9, 2012
ReceivedApr 16, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K121142

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.