ClearanceBrief
510(k) K083833 ยท DQY Catheter, Percutaneous

ENABLER-P CATHETER, 1000 PART NUMBER:1160

ApplicantEndocross, Ltd., Washington DC, US
DecisionSubstantially Equivalent, May 22, 2009
ReceivedDec 23, 2008
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K083833

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.