ClearanceBrief
510(k) K965256 ยท GFD Dermatome

DMS-1000C DERMOABRADER

ApplicantMattioli Engineering, Srl, Florence, IT
DecisionSubstantially Equivalent, Dec 9, 1996
ReceivedAug 16, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K965256

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.