ClearanceBrief
510(k) K230571 ยท DSA Cable, Transducer And Electrode, Patient, (Including Connector)

RFP-100A Connector Cable (Single Use)

ApplicantBaylis Medical Technologies, Inc., Mississauga, CA
DecisionSubstantially Equivalent, May 30, 2023
ReceivedMar 1, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230571

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.