ClearanceBrief
510(k) K990240 ยท KLX Electroglottograph

ELECTROGLOTTOGRAPH

ApplicantKay Elemetrics Corp., Lincoln Park NJ, US
DecisionSubstantially Equivalent, Mar 11, 1999
ReceivedJan 25, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K990240

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.