ClearanceBrief
510(k) K083556 ยท MND Ligator, Esophageal

MODIFICATION TO AUTO-BAND LIGATOR

ApplicantScandimed International, Jamestown RI, US
DecisionSubstantially Equivalent, Feb 19, 2009
ReceivedDec 2, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K083556

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.