ClearanceBrief
510(k) K001390 ยท DSA Cable, Transducer And Electrode, Patient, (Including Connector)

BIOSENSE WEBSTER PATIENT CABLE AND LEADWIRES

ApplicantBiosense Webster, Inc., Diamond Bar CA, US
DecisionSubstantially Equivalent, Jul 21, 2000
ReceivedMay 2, 2000
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K001390

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.