ClearanceBrief
510(k) K132535 ยท MND Ligator, Esophageal

AUTOBAND LIGATOR

ApplicantEndochoice, Inc., Alpharetta GA, US
DecisionSubstantially Equivalent, Aug 23, 2013
ReceivedAug 13, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K132535

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.