ClearanceBrief
510(k) K770559 ยท DXY Implantable Pacemaker Pulse-Generator

C-L0L CARDIAC PACEMAKER

ApplicantCoratomic, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 28, 1977
ReceivedMar 23, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770559

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.