ClearanceBrief
510(k) K840047 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)

LIFEPAK 7D

ApplicantPhysio-Control Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 4, 1984
ReceivedJan 6, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K840047

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.