ClearanceBrief
510(k) K884122 ยท DXG Computer, Diagnostic, Pre-Programmed, Single-Function

TYPE 9320 CARDIAC OUTPUT SYSTEM ATHENA

ApplicantS & W Medico Teknik, Denmark, DK
DecisionSubstantially Equivalent, Apr 25, 1989
ReceivedSep 30, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884122

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.