ClearanceBrief
510(k) K170759 ยท KTI Bronchoscope Accessory

CRE Pulmonary Balloon Dilatation Catheter

ApplicantBoston Scientific Corporation, Marlboro MA, US
DecisionSubstantially Equivalent, Jun 23, 2017
ReceivedMar 13, 2017
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K170759

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.