ClearanceBrief
510(k) K843808 ยท OLT Non-Normalizing Quantitative Electroencephalograph Software

DUAL CHENNEL BRAIN ACTIVITY MONITOR

ApplicantDatex Division Instrumentarium Corp., Helsinki 10 Finland, US
DecisionSubstantially Equivalent, Nov 8, 1984
ReceivedSep 27, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K843808

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.