ClearanceBrief
510(k) K853058 ยท DXY Implantable Pacemaker Pulse-Generator

NEOS - M ABP

ApplicantBiotronik Sales, Inc., Lake Oswego OR, US
DecisionSubstantially Equivalent, Sep 13, 1985
ReceivedJul 19, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K853058

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.