ClearanceBrief
510(k) K861710 ยท DXK Echocardiograph

MODEL UST-SSD 880L1-5 TRANESOPHAGEAL PHASED ARRAY

ApplicantJohnson & Johnson Professionals, Inc., Ramsey NJ, US
DecisionSubstantially Equivalent, Jul 9, 1986
ReceivedMay 5, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K861710

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.