ClearanceBrief
510(k) K013005 ยท HCA Catheter, Ventricular

ACT 11 MP VENTRICULAR CATHETER

ApplicantInnerspace, Inc., Santa Ana CA, US
DecisionSubstantially Equivalent, Mar 8, 2002
ReceivedSep 6, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K013005

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.