ClearanceBrief
510(k) K023591 ยท DQO Catheter, Intravascular, Diagnostic

ULTRA HIGH PRESSURE INJECTOR LINES

ApplicantDeroyal Industries, Inc., Powell TN, US
DecisionSubstantially Equivalent, Jun 18, 2003
ReceivedOct 25, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K023591

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.