ClearanceBrief
510(k) K030398 ยท DQR Cannula, Catheter

CARDIACASSIST TRANSSEPTAL CANNULA SET, MODEL 5132-6221

ApplicantCardiacassist, Inc., Pittsburgh PA, US
DecisionSubstantially Equivalent, May 23, 2003
ReceivedFeb 6, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030398

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.