ClearanceBrief
510(k) K003020 ยท DQO Catheter, Intravascular, Diagnostic

CARDIAC FUNCTION LABORATORY; PRESSURE INTERFACE; PRESSURE / VOLUME CATHETER

ApplicantCd Leycom BV, Zoetermeer, NL
DecisionSubstantially Equivalent, May 11, 2001
ReceivedSep 27, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K003020

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.