ClearanceBrief
510(k) K812160 ยท GES Blade, Scalpel

MICROSURGICAL BLADE

ApplicantVxtra Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Aug 31, 1981
ReceivedJul 29, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812160

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.