ClearanceBrief
510(k) K920492 ยท DYN Mouthpiece, Saliva Ejector

HIGH VAC

ApplicantHygoplastic, Inc., Grafton WI, US
DecisionSubstantially Equivalent, May 11, 1992
ReceivedFeb 3, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920492

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.