ClearanceBrief
510(k) K891383 ยท OLZ Automatic Event Detection Software For Polysomnograph With Electroencephalograph

MEDILOG 9200 EEG REPLAY/ANALYSIS SYSTEM

ApplicantOxford Medilog, Inc., Clearwater FL, US
DecisionSubstantially Equivalent, Jun 1, 1989
ReceivedMar 9, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K891383

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.