ClearanceBrief
510(k) K110140 ยท GWF Stimulator, Electrical, Evoked Response

NEUROVISION NERVE LOCATOR MONITOR

ApplicantNeurovision Medical Products, Inc., Ventura CA, US
DecisionSubstantially Equivalent, Sep 30, 2011
ReceivedJan 18, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K110140

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.