ClearanceBrief
510(k) K093903 ยท KRH Ring, Annuloplasty

ATS TRI-AD SEMI-FLEXIBLE TRICUSPID ANUULOPLASTY, MODEL 900SFC

ApplicantGenesee Biomedical, Inc., Denver CO, US
DecisionSubstantially Equivalent, Jul 15, 2010
ReceivedDec 22, 2009
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K093903

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.