ClearanceBrief
510(k) K182327 ยท DSA Cable, Transducer And Electrode, Patient, (Including Connector)

Patient Cables and Leadwires , Disposable ECG Leadwires

ApplicantOrantech, Inc., Shenzhen, CN
DecisionSubstantially Equivalent, Jan 30, 2019
ReceivedAug 27, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K182327

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.