ClearanceBrief
510(k) K841832 ยท KLX Electroglottograph

GLOTTAL FREQUENCY ANALYSER

ApplicantTeltec Electronic Equipment AB, Mchenry IL, US
DecisionSubstantially Equivalent, Jul 18, 1984
ReceivedMay 3, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K841832

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.