ClearanceBrief
510(k) K112052 ยท GWF Stimulator, Electrical, Evoked Response

CAREFUSION NICOLET EDX

ApplicantCarefusion 209, Inc., Middleton WI, US
DecisionSubstantially Equivalent, Mar 15, 2012
ReceivedJul 18, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K112052

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.