ClearanceBrief
510(k) K801224 ยท DXK Echocardiograph

CAMBRIDGE CARDIAC DIAGNOSTIC SYSTEM

ApplicantCambridge Instruments, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jun 26, 1980
ReceivedMay 22, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K801224

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.