ClearanceBrief
510(k) K934783 ยท EIA Unit, Operative Dental

KAVO INTRASEPT 905

ApplicantKavo America, Lake Zurich IL, US
DecisionSubstantially Equivalent, May 16, 1994
ReceivedOct 6, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K934783

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.