ClearanceBrief
510(k) K213007 ยท OLV Standard Polysomnograph With Electroencephalograph

Cerebra Sleep System

ApplicantCerebra Medical , Ltd., Winnipeg, CA
DecisionSubstantially Equivalent, Jul 6, 2022
ReceivedSep 20, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K213007

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.