ClearanceBrief
510(k) K922488 ยท IKN Electromyograph, Diagnostic

PHASIS ELECTROMYOGRAPH

ApplicantBiosound, Inc., San Jose CA, US
DecisionSubstantially Equivalent, Mar 2, 1993
ReceivedMay 27, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922488

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.