ClearanceBrief
510(k) K863011 ยท

DENTATUS LS/EUROFLEX F-IV/ISOLIGHT REFLECT/CM-II

ApplicantSds Dental, Inc., Washington DC, US
DecisionSubstantially Equivalent, Oct 10, 1986
ReceivedAug 8, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863011

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.