ClearanceBrief
510(k) K974683 ยท DQY Catheter, Percutaneous

NAVIPORT DEFLECTABLE TIP GUIDING CATHETER

ApplicantCardima, Inc., Fremont CA, US
DecisionSubstantially Equivalent, Jun 22, 1999
ReceivedDec 16, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K974683

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.