ClearanceBrief
510(k) K002708 ยท KOJ Airbrush

KAVO CORUND HANDPIECE 2013

ApplicantKavo America, Lake Zurich IL, US
DecisionSubstantially Equivalent, Nov 28, 2000
ReceivedAug 30, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K002708

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.