ClearanceBrief
510(k) K023174 ยท LDF Electrode, Pacemaker, Temporary

DISPOSABLE TEMPORARY PACING WIRE

ApplicantRiver Medical, Inc., Portland OR, US
DecisionSubstantially Equivalent, Jun 11, 2003
ReceivedSep 23, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K023174

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.