ClearanceBrief
510(k) K221464 ยท DXX System, Catheter Control, Steerable

CorPath GRX System

ApplicantCorindus, Inc., Waltham MA, US
DecisionSubstantially Equivalent, Jul 27, 2022
ReceivedMay 19, 2022
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K221464

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.