ClearanceBrief
510(k) K854233 ยท DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)

CMI 3000

ApplicantCardio Management, Inc., Birmingham AL, US
DecisionSubstantially Equivalent, Jan 8, 1986
ReceivedOct 21, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854233

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.