ClearanceBrief
510(k) K933874 ยท HQZ Frame, Spectacle

SPECTACLE FRAME

ApplicantDesigner Frames, Miami FL, US
DecisionSubstantially Equivalent, Sep 20, 1993
ReceivedAug 6, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K933874

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.