ClearanceBrief
510(k) K770756 ยท DXK Echocardiograph

ECHOCARDIOGRAPHY SYS., MODEL 3860

ApplicantHoneywell, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, May 9, 1977
ReceivedApr 25, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770756

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.