ClearanceBrief
510(k) K853769 ยท DXK Echocardiograph

IRREGULAR CURVE TRACING REVISITION & DOPPLER

ApplicantHewlett-Packard Co., Andover MA, US
DecisionSubstantially Equivalent, Oct 31, 1985
ReceivedSep 9, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K853769

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.