ClearanceBrief
510(k) K950989 ยท DPS Electrocardiograph

CARDIOSMART

ApplicantHellige GmbH, D7800 Freiburg Im Breisga, DE
DecisionSubstantially Equivalent, May 13, 1996
ReceivedMar 3, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K950989

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.