ClearanceBrief
510(k) K181000 ยท DQY Catheter, Percutaneous

SelectFlex 072 Neurovascular Access System

ApplicantQ'Apel, Santa Monica CA, US
DecisionSubstantially Equivalent, Sep 13, 2018
ReceivedApr 16, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K181000

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.