ClearanceBrief
510(k) K093236 ยท KNQ Dilator, Esophageal

ETHICON ENDO-SURGERYOPTICAL DILATOR

ApplicantEthicon Endo-Surgery, Inc., Cincinnati OH, US
DecisionSubstantially Equivalent, Nov 10, 2009
ReceivedOct 15, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K093236

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.