ClearanceBrief
510(k) K140485 ยท DQX Wire, Guide, Catheter

MANDREL GUIDEWIRE

ApplicantLake Region Medical, Chaska MN, US
DecisionSubstantially Equivalent, Mar 27, 2014
ReceivedFeb 26, 2014
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K140485

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.