ClearanceBrief
510(k) K113074 ยท IKN Electromyograph, Diagnostic

CMAP PRO

ApplicantMedical Technologies, Inc., Albuquerque NM, US
DecisionSubstantially Equivalent, Feb 2, 2012
ReceivedOct 17, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K113074

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.