ClearanceBrief
510(k) K240377 · DSA Cable, Transducer And Electrode, Patient, (Including Connector)

LIFEPAK® ECG Cables

ApplicantStryker Physio-Control, Redmond WA, US
DecisionSubstantially Equivalent, May 7, 2024
ReceivedFeb 7, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K240377

DateFirm and productCodeLinked 510(k)
Feb 5, 2025Physio-Control, Inc.
LIFEPAK 35 ECG cable REF 11111-000041
Open, Classified
DSANone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.