ClearanceBrief
510(k) K782149 ยท DXY Implantable Pacemaker Pulse-Generator

PULSE GENERATOR, IMPLANTABLE CARDIAC

ApplicantTelectronics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 8, 1979
ReceivedDec 26, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K782149

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.