ClearanceBrief
510(k) K934009 ยท DQY Catheter, Percutaneous

ACS POWERGUIDE CORONARY GUIDING CATHETER

ApplicantAdvanced Cardiovascular Systems, Inc., Temecula CA, US
DecisionSubstantially Equivalent, Jan 11, 1994
ReceivedAug 18, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K934009

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.