ClearanceBrief
510(k) K865031 ยท DPS Electrocardiograph

ELECTROCARDIOGRAPH

ApplicantNihon Kohden America, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Feb 19, 1987
ReceivedDec 23, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K865031

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.