ClearanceBrief
510(k) K112886 ยท DQY Catheter, Percutaneous

UPSTREAM SUPPORT CATHETER

ApplicantUpstream Peripheral Technologies, Philedelphia PA, US
DecisionSubstantially Equivalent, Feb 23, 2012
ReceivedSep 30, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K112886

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.