ClearanceBrief
510(k) K893995 ยท KGS Retention Device, Suture

DERMACARE TIE HOLDER

ApplicantDermacare, Louisville KY, US
DecisionSubstantially Equivalent, Aug 11, 1989
ReceivedJun 5, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K893995

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.