ClearanceBrief
510(k) K990031 ยท LOS

NIHON KOHDEN ECG-9010K AND ECG-9020K CARDIOFAX GEM AND ACCESSORIES

ApplicantNihon Kohden America, Inc., Irvine CA, US
DecisionSubstantially Equivalent, Apr 16, 1999
ReceivedJan 5, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K990031

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.