ClearanceBrief
510(k) K800782 ยท KRE Analyzer, Pacemaker Generator Function, Indirect

PACE-PULSE/COMPUTRAC

ApplicantBib, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, May 28, 1980
ReceivedApr 8, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800782

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.