ClearanceBrief
510(k) K152991 ยท DQX Wire, Guide, Catheter

OptoWire Deux

ApplicantOpsens, Quebec, CA
DecisionSubstantially Equivalent, Feb 11, 2016
ReceivedOct 13, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K152991

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.