ClearanceBrief
510(k) K984504 ยท LOS

NIHON KOHDEN ECG-9110K AND ECG-9130K CARDIOFAX Q AND ACCESSORIES

ApplicantNihon Kohden America, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Apr 15, 1999
ReceivedDec 18, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K984504

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.