ClearanceBrief
510(k) K802670 ยท DXK Echocardiograph

CONTIUOUS WAVE DOPPLER ULTRASOUND

ApplicantAmerican Edwards Laboratories, Walker MI, US
DecisionSubstantially Equivalent, Nov 26, 1980
ReceivedOct 27, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802670

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.