ClearanceBrief
510(k) K901609 ยท KLX Electroglottograph

ELECTROGLOTTOGRAPH

ApplicantGlottal Ent., Inc., Washington DC, US
DecisionSubstantially Equivalent, Jun 28, 1990
ReceivedApr 6, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K901609

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.