ClearanceBrief
510(k) K864507 ยท LDF Electrode, Pacemaker, Temporary

V-PACE(TM) TRANSLUMINAL VENTRICULAR/ MODEL SP5540

ApplicantSpectramed, Inc., Findley MN, US
DecisionSubstantially Equivalent, Mar 6, 1987
ReceivedNov 14, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K864507

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.