ClearanceBrief
510(k) K864408 ยท IKN Electromyograph, Diagnostic

EMG-1, MOTOR NERVE MONITOR

ApplicantAlgotek, Inc., Palo Alto CA, US
DecisionSubstantially Equivalent, Jan 30, 1987
ReceivedNov 10, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K864408

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.