ClearanceBrief
510(k) K851900 ยท DTC Analyzer, Pacemaker Generator Function

SEA MED DDD PACING SYSTEM ANALYZER

ApplicantSeamed Corp., Redmond WA, US
DecisionSubstantially Equivalent, Jul 19, 1985
ReceivedApr 30, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K851900

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.