ClearanceBrief
510(k) K961636 ยท OLZ Automatic Event Detection Software For Polysomnograph With Electroencephalograph

MEDILOG VISION

ApplicantOxford Instruments, Plc., Clearwater FL, US
DecisionSubstantially Equivalent, Jan 17, 1997
ReceivedApr 29, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961636

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.