ClearanceBrief
510(k) K020079 ยท HNO Keratome, Ac-Powered

BLADEWORKS MICROKERATOME BLADE, MODEL 7061

ApplicantBlade Works, Inc., San Marcos CA, US
DecisionSubstantially Equivalent, Apr 19, 2002
ReceivedJan 10, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K020079

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.