ClearanceBrief
510(k) K943913 ยท HQZ Frame, Spectacle

MAX FRAME DESIGN

ApplicantNoble Optic, Herdon VA, US
DecisionSubstantially Equivalent, Sep 7, 1994
ReceivedAug 11, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K943913

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.