ClearanceBrief
510(k) K984258 ยท DQO Catheter, Intravascular, Diagnostic

NEUROVASX SUB-MICROINFUSION CATHETER

ApplicantNeuro Vasx, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, Feb 11, 1999
ReceivedNov 30, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K984258

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.