ClearanceBrief
510(k) K193380 ยท NRY Catheter, Thrombus Retriever

CERENOVUS Large Bore Catheter; CERENOVUS Aspiration Tubing Set

ApplicantCodman & Shurtleff, Inc., Raynham MA, US
DecisionSubstantially Equivalent, Jul 20, 2020
ReceivedDec 5, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K193380

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.