ClearanceBrief
510(k) K900220 ยท DTE Pulse-Generator, Pacemaker, External

TRANS-PACE 100

ApplicantSynchromed Corp., Cape Coral FL, US
DecisionSubstantially Equivalent, Jul 17, 1990
ReceivedJan 17, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900220

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.