ClearanceBrief
510(k) K060572 ยท DQY Catheter, Percutaneous

MODIFICATION TO POLARCATH PERIPHERAL DILATATION SYSTEM

ApplicantBoston Scientific Corporation, Los Gatos CA, US
DecisionSubstantially Equivalent, Mar 15, 2006
ReceivedMar 6, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K060572

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.