ClearanceBrief
510(k) K130238 ยท OMA Amplitude-Integrated Electroencephalograph

NIHON KOHDEN AE-918P NEURO UNIT

ApplicantNihon Kohden Corp., San Diego CA, US
DecisionSubstantially Equivalent, Mar 4, 2015
ReceivedJan 31, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K130238

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.