ClearanceBrief
510(k) K161640 ยท NRY Catheter, Thrombus Retriever

Penumbra System ACE 68 Reperfusion Catheter

ApplicantPenumbra, Inc., Alameda CA, US
DecisionSubstantially Equivalent, Jul 12, 2016
ReceivedJun 14, 2016
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K161640

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.