ClearanceBrief
510(k) K800088 ยท DTE Pulse-Generator, Pacemaker, External

PACEMAKER ELECTRODE INSERTER AIDE

ApplicantTelectronics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 29, 1980
ReceivedJan 14, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800088

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.