ClearanceBrief
510(k) K931972 ยท HQZ Frame, Spectacle

FRAME - SPECTACLE

ApplicantEyetel Optics, Inc., Miami FL, US
DecisionSubstantially Equivalent, Oct 1, 1993
ReceivedApr 22, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K931972

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.