ClearanceBrief
510(k) K874090 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)

300M ECG MONITRO/TRANSCUTANEOUS PACEMAKER

ApplicantMedac, Inc., Tualatin OR, US
DecisionSubstantially Equivalent, Dec 15, 1987
ReceivedOct 7, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874090

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.