ClearanceBrief
510(k) K880217 ยท DXK Echocardiograph

SSD-870 CARDIO VASCULAR PHASED ARRAY SECTOR SCANN.

ApplicantGe Medical Systems Information Technologies, Wallingford CT, US
DecisionSubstantially Equivalent, Apr 25, 1988
ReceivedJan 20, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880217

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.