ClearanceBrief
510(k) K812526 ยท GES Blade, Scalpel

MICRO BLADE II

ApplicantVxtra Corp., Walker MI, US
DecisionSubstantially Equivalent, Sep 16, 1981
ReceivedSep 2, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812526

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.