ClearanceBrief
510(k) K173761 ยท NRY Catheter, Thrombus Retriever

Penumbra System Reperfusion Catheter JET 7

ApplicantPenumbra, Inc., Alameda CA, US
DecisionSubstantially Equivalent, Aug 17, 2018
ReceivedDec 11, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K173761

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.