ClearanceBrief
510(k) K895728 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)

R2 PACE ADAPTOR CABLE, MODEL 196

ApplicantDarox Corp., Niles IL, US
DecisionSubstantially Equivalent, Oct 12, 1989
ReceivedSep 25, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895728

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.