ClearanceBrief
510(k) K024000 ยท DQO Catheter, Intravascular, Diagnostic

METRICATH SYSTEM COMPRISED OF METRICATH 1000 CONSOLE & METRICATH BALLOON CATHETER

ApplicantAngiometrx, Inc., Seattle WA, US
DecisionSubstantially Equivalent, Jun 26, 2003
ReceivedDec 4, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K024000

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.