ClearanceBrief
510(k) K821090 ยท DPS Electrocardiograph

CARDI-O-LIFE MODEL 8823

ApplicantAmertek, Mchenry IL, US
DecisionSubstantially Equivalent, Jul 8, 1982
ReceivedApr 19, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K821090

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.