ClearanceBrief
510(k) K863878 ยท DXY Implantable Pacemaker Pulse-Generator

TRIOS-M VS-1 PULSE GENERATOR

ApplicantBiotronik Sales, Inc., Lake Oswego OR, US
DecisionSubstantially Equivalent, Dec 10, 1986
ReceivedOct 6, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863878

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.