ClearanceBrief
510(k) K140356 ยท DQO Catheter, Intravascular, Diagnostic

SUMMED HIGH PRESSURE LINE

ApplicantSunny Medical Device (Shenzhen) Co., Ltd., Irvine CA, US
DecisionSubstantially Equivalent, Mar 20, 2015
ReceivedFeb 12, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K140356

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.