ClearanceBrief
510(k) K911332 ยท HQZ Frame, Spectacle

SPECTACLE FRAME

ApplicantAustralian Optical Co., Inc., Kansas City MO, US
DecisionSubstantially Equivalent, May 6, 1991
ReceivedMar 26, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K911332

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.