ClearanceBrief
510(k) K780332 ยท DXK Echocardiograph

CATHODE RAY TUBE DISPLAY MODEL 1340A

ApplicantHewlett-Packard Co., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 22, 1978
ReceivedFeb 28, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780332

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.