ClearanceBrief
510(k) K001800 ยท IKN Electromyograph, Diagnostic

ACCUWARM EMG HEAT LAMP

ApplicantRjl Associates, LLC, Waterford CT, US
DecisionSubstantially Equivalent, Sep 12, 2000
ReceivedJun 14, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K001800

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.